B cells in X linked lymphoproliferativedisease journal J. Clin. Invest. volume 116 issue 2 pages 322 ...Infobox disease Name X linked lymphoproliferativedisease Image Caption DiseasesDB 3998 ICD10 ICD10 D 82 3 d 80 ICD9 ICDO OMIM 308240 OMIM mult OMIM2 300635 MedlinePlus eMedicineSubj med eMedicineTopic 1370 MeshID D008232 X linked lymphoproliferativedisease also known as Duncan s disease ref name Andrews cite book author James, William D. Berger, Timothy G. et al. title Andrews Diseases of the Skin ... doi accessdate ref rp 86 or Purtilo syndrome ref http ghr.nlm.nih.gov condition x linked lymphoproliferativedisease ref is a lymphoproliferative disorder . ref name Bolognia cite book author Rapini, Ronald ... as X linked familial hemophagocytic lymphohistiocytosis instead of X linked lymphoproliferativedisease ... and not as X linked lymphoproliferativedisease journal Blood volume 116 issue 7 pages ... External links http www.rareshare.org communities x linked lymphoproliferativedisease X linked lymphoproliferativedisease community http www.xlpresearchtrust.org XLP Research Trust http www.ncbi.nlm.nih.gov bookshelf br.fcgi?book gene&part x lpd GeneReview NIH UW entry on LymphoproliferativeDisease ... on the X chromosome that has been found to be associated with a T and NK cell lymphoproliferative ... name titleX linked Lymphoproliferative Syndrome Immunodeficiency Disorders Merck Manual Professional cite web url http www.merck.com mmpe sec13 ch164 ch164p.html title X linked Lymphoproliferative Syndrome ... lymphoproliferative syndrome journal Nature volume 444 issue 7115 pages 110 4 year 2006 month November ... Presentation Strangely, in boys with X linked lymphoproliferative disorder, there is an inability to mount ... between EBV and X linked lymphoproliferative disorder is yet to be determined. ref name item14 Winter, S.S. Lymphoproliferative disorders. Emedicine. December 20, 2006. http www.emedicine.com ... B cell s. ref name pmid16424938 cite journal author Ma CS, Pittaluga S, Avery DT, et al. title Selective ... more details
Infobox Disease Name Lymphoproliferative disorders Image Caption DiseasesDB ICD10 ICD9 ICD9 238.79 ICDO OMIM MedlinePlus eMedicineSubj ped eMedicineTopic 1345 MeshID D008232 Lymphoproliferative disorders ... linked Lymphoproliferative disorder main X linked lymphoproliferativedisease There is a mutation on the X chromosome that has been found to be associated with a T cell and NK cell lymphoproliferative disorder. Autosomal lymphoproliferative disorder main Autoimmune lymphoproliferative syndrome Some children with autoimmune lymphoproliferative disorders are heterozygous for a mutation in the gene that codes ... transplantation and immunosuppressant therapies. In most reported cases, these cause B cell lymphoproliferative ... disorders , but technically Lymphoproliferative disorders are a subset of immunoproliferative ... s multiple myeloma Waldenstrom s macroglobulinemia Wiskott Aldrich syndrome post transplant lymphoproliferative disorder Autoimmune lymphoproliferative syndrome ALPS Lymphoid interstitial pneumonia ... Lymphoproliferative disorders are a set of disorders characterized by the abnormal proliferation of lymphocyte s into a monoclonal lymphocytosis . The two major types of lymphocytes are B cells and T cells ... have some sort of immunodysfuction are susceptible to developing a lymphoproliferative disorder because ... gene mutations that have been identified to cause lymphoproliferative disorders, however there are also acquired and iatrogenic causes. ref name item14 Winter, S.S. Lymphoproliferative disorders ..., and are predisposed to develop a lymphoproliferative disorder or lymphoma. Children with common variable immune deficiency CVID are also at a higher risk of developing a lymphoproliferative disorder. Some disorders that predispose a person to lymphoproliferative disorders are severe combined immuno ... disorder, people who are heterozygote s for this still have an increased risk of developing a lymphoproliferative ... of lymphoproliferative disorders. The most common is congenital HIV infection because it is highly associated ... more details
response that entails rapid T cell replication. Standard antigens , such as tetanus toxoid , that elicit this response are used in lab tests of immune competence http cancerweb.ncl.ac.uk cgi bin omd?lymphoproliferative response . External links http cancerweb.ncl.ac.uk cgi bin omd?lymphoproliferative response Online Medical Dictionary, lymphoproliferative response med stub Category Immune system ... more details
Infobox Disease Name Post transplant lymphoproliferative disorder Image Caption DiseasesDB 34154 ICD10 ICD9 ICD9 238.77 ICDO M9970 1 OMIM MedlinePlus eMedicineSubj ped eMedicineTopic 2851 MeshID Post transplant lymphoproliferative disorder PTLD is the name given to a B cell proliferation due to therapeutic immunosupression after organ transplantation. These patients may develop infectious mononucleosis like lesions or polyclonal polymorphic B cell hyperplasia. Some of these B cells may undergo mutations which will render them malignant, giving rise to a lymphoma . cn date June 2011 In some patients, the malignant cell clone can become the dominant proliferating cell type, leading to frank lymphoma, a group of B cell lymphoma s occurring in Immunosuppression immunosuppressed patients following organ transplant . Causes The disease is an uncontrolled proliferation of B cell lymphocytes following infection with Epstein Barr virus . ref name pmid15660500 cite journal author Gottschalk S, Rooney CM, Heslop HE title Post transplant lymphoproliferative disorders journal Annu. Rev. Med. volume 56 issue 1 pages 29 44 year 2005 pmid 15660500 doi 10.1146 annurev.med.56.082103.104727 url http arjournals.annualreviews.org doi abs 10.1146 annurev.med.56.082103.104727?url ver Z39.88 2003&rfr id ori rid crossref.org&rfr dat cr pub 3dncbi.nlm.nih.gov ref Production of an interleukin 10 , an endogenous anti T cell cytokine , has also been implicated. In immunocompetent patients, Epstein Barr virus causes infectious mononucleosis , characterised by a proliferation of B lymphocytes which is controlled ... in organ transplantation inhibit T cell function, and can prevent the control of the B ... lymphoproliferative disorder. Such antibodies include Anti thymocyte globulin ATG , Anti lymphocyte ... Post Transplant Lymphoproliferative Disorder Categories Category Transplantation medicine Category Lymphoma Other languages de Lymphoproliferative Erkrankung nach Transplantation ... more details
Infobox Disease Name Autoimmune lymphoproliferative syndrome Image Caption DiseasesDB 33425 DiseasesDB ... doi 10.1182 blood 2006 01 010124 pmc 1895548 title Rapamycin improves lymphoproliferativedisease ... disease in MRL lpr mice or in patients with autoimmune lymphoproliferative syndrome pages 1049 55 pmid ... eMedicineTopic MeshID Autoimmune lymphoproliferative syndrome is a form of lymphoproliferative disorder ... Lymphoproliferative Syndrome Lymphoproliferative disorders ALPS is a rare disorder of abnormal ... on activated B and T lymphocytes and Fas ligand on activated T lymphocytes. Fas and Fas ligand interact ... pathway, leading to chronic non malignant lymphoproliferation, autoimmune disease, and secondary ... tends to present at a young age median 11.5 months and may improve with age. Autoimmune disease ... if driver of disease or epiphenomenon May be falsely elevated in setting of lymphopenia or falsely ... prose section date December 2011 Mostly commonly directed at autoimmune disease Maybe needed ... disease Some patients have partial responses Some patients relapse Does not affect lymphoproliferation ... agent in clinical trials Most patients have complete resolution of autoimmune disease 90 ref name pmid19208097 ... lymphadenopathy and splenomegaly 90 Some patients have near complete response disease flares ... autoimmune disease Most patients have elimination of peripheral blood DNTs mTOR Akt PI3K pathway may ... in patients that require chronic therapy. Better activity against autoimmune disease and lymphoproliferation ... lymphoproliferative syndrome An experiment of nature involving lymphocyte apoptosis year ... title Causes and consequences of the autoimmune lymphoproliferative syndrome year 2006 last1 Rao ... in the management and understanding of autoimmune lymphoproliferative syndrome ALPS year 2010 last1 ... response reveal autoimmune lymphoproliferative syndrome ALPS year 2005 last1 Teachey first1 ... with Autoimmune Lymphoproliferative Syndrome year 2002 last1 Bleesing first1 Jack J.H. last2 Brown ... more details
Infobox television episode Title The Disease Image Image ST VOY The Disease.jpg 270px Caption Harry Kim becomes intimate with Varro scientist Tal Series Star Trek Voyager Season 5 Episode 17 Production 210 Airdate February 24, 1999 Writer Kenneth Biller br Michael Taylor screenwriter Michael Taylor Director David Livingston director David Livingston Guests Musetta Vander as Tal br Charles Rocket as Jippeq Prev Dark Frontier Next Course Oblivion Star Trek Voyager Course Oblivion Episode list List of Star Trek Voyager episodes List of Star Trek Voyager episodes NOTOC for an abnormal condition affecting the body of an organism Disease The Disease is an episode of Star Trek Voyager , the 17th episode of the fifth season. The episode had an average rating of 4.2 5 on the official Star Trek website as of August 23, 2007 . http www.startrek.com startrek view series VOY episode 104851.html Plot Voyager stops to assist a xenophobic species known as the Varro. This species lives on a Generation ship generational ship which has housed them for 400 years. While the crew works on the Varro ship, Voyager is infested with synthetic ship eating parasites that had been released on the Varro ship by dissident Varro. Meanwhile, Harry Kim Star Trek Harry Kim becomes intimate with Varro scientist Tal, and develops a physiological bond with her, one that is standard in the Varro. The physiological connection alters his behavior and sways him from his duties aboard Voyager . It is later revealed that Tal is one of the separatists. There has been a rumour of a minority of Varro that want off the ship. The parasites that Tal helped create were made to separate the individual pods of the Varro ship without destroying the ship itself. Fractures along the hull created by the parasites begin to grow as the Varro ship begins to fall apart. Voyager s docking port is seized, trapping it with the Varro ... Trek VOY Star Trek DEFAULTSORT Disease, The Category Star Trek Voyager episodes Category 1999 television ... more details
Infobox disease Name Castleman s disease Image Castleman disease high mag.jpg Caption Micrograph of Castleman s disease, hyaline vascular variant, exhibiting the characteristically expanded mantle zone ... ICD9 ICD9 785.6 ICDO OMIM MedlinePlus eMedicineSubj eMedicineTopic MeshID D005871 Castleman s disease ... is an uncommon lymphoproliferative disorder that can involve single lymph node stations or can ... Castleman s Disease journal Onkologie date 23 year 2011 month August volume 34 issue 8 9 pages 456 458 ... F, Huber O, Morel P title Surgical management of abdominal and retroperitoneal Castleman s disease ... B cell s that often produce cytokine s. While not officially considered a cancer, the overgrowth of lymphocytes with this disease is similar to lymphoma. ref cite web title Castleman disease publisher Mayo Clinic url http www.mayoclinic.com health castleman disease DS01000 accessdate 2010 02 ... journal author Castleman B, Iverson L, Menendez VP title Localized mediastinal lymphnode hyperplasia ... 1097 0142 195607 08 9 4 822 AID CNCR2820090430 3.0.CO 2 4 url ref Types Image Castleman disease intermed mag.jpg thumb right Intermediate magnification micrograph of Castleman disease showing the characteristic ... of Castleman s disease. In most of the cases, Castleman s disease is likely due to hypersecretion of the cytokine Interleukin 6 IL 6 , ref name pmid17766835 cite journal author Ahmed B, Tschen JA, Cohen PR, et al. title Cutaneous castleman s disease responds to anti interleukin 6 treatment journal ... Unicentric Castleman s disease involves tissue growths at only a single site. It usually ..., in 2011, Weng et al. described a patient with unicentric Castleman s disease, hyaline vascular ... of Castleman s disease. ref name pmid21934347 Multicentric Castleman s disease MCD involves growths ... Castleman s disease a case report journal J Med Case Reports volume 1 issue pages 78 year .... The form of MCD most closely associated with KSHV is the plasmacytic form of Castleman s disease while ... more details
Infobox disease Name Myeloproliferative disease Image Caption ICD10 ICD10 D 47 1 d 37 ICD9 ICD9 205.1 , ICD9 238.4 , ICD9 289.89 , ICD9 289.9 ICDO 9950 0 9964 3 OMIM DiseasesDB MedlinePlus eMedicineSubj eMedicineTopic MeshID D009196 The myeloproliferative diseases MPDs , myeloproliferative neoplasms, MPNs are a group of diseases of the bone marrow in which excess cells are produced. They are related to, and may evolve into, myelodysplastic syndrome and acute myeloid leukemia , although the myeloproliferative diseases on the whole have a much better prognosis than these conditions. The concept of myeloproliferative disease was first proposed in 1951 by the eminent hematologist William Dameshek . ref cite journal author Dameshek W title Some speculations on the myeloproliferative syndromes journal Blood volume 6 issue 4 pages 372 5 year 1951 pmid 14820991 ref In the most recent World Health Organization classification of Hematologic malignancies, this group of diseases was renamed from myeloproliferative ... clonal genetic changes that are a salient feature of this group of disease. Classification Although ... of the myeloid lineage in the bone marrow. The lymphoid lineage may produce similar diseases, the lymphoproliferative ... level, vitamin B sub 12 sub or B sub 12 sub binding capacity and serum urate. ref cite book author ... publisher W B Saunders location London year 2001 isbn 0 443 06377 X page 586 ref According ... leads to CML with usual neutrophilia and basophilia br b. minor BCR ABL p190 leads to CML which has a tendency to become acute lymphoblastic leukemia ALL usually precursor B ALL and rarely precursor ... fibrosis, and increased myeloid precursors br b. Fibrotic phase collagenous fibrosis with lack of marrow ..., and increased myeloid and erythroid precursors br b. Fibrotic phase collagenous fibrosis with lack ... megakaryocytes with fibrosis and little increase in other bone marrow elements br b. Fibrotic phase ... DEFAULTSORT Myeloproliferative Disease Category Myeloid neoplasia ar de Myeloproliferative ... more details
B title Is celiac disease an autoimmune disorder? journal Curr. Opin. Immunol. volume 17 issue ...expert subject 1 Medicine date November 2011 Infobox disease Name Autoimmune diseases Image Caption DiseasesDB ... places e.g. Goodpasture s disease which may affect the basement membrane in both the lung and the kidney ... which decreases the immune response. Criteria For a disease to be regarded as an autoimmune disease ... T cells Indirect evidence based on reproduction of the autoimmune disease in experimental animals ... type III , or Type IV hypersensitivity type IV . No type of autoimmune disease mimics ... accessdate ref There is an on going discussion about when a disease should be considered autoimmune ... ADEM Accepted ref name Mesh MeshName Autoimmune Diseases ref Addison s Disease interferon ... liver antigen Autoimmune inner ear disease Accepted ref name urlAutoimmune Inner Ear Disease cite web url http www.bcm.edu oto grand 4893.html title Autoimmune Inner Ear Disease, Baylor College of Medicine year 1993 ref Autoimmune lymphoproliferative syndrome Accepted TNFRSF6 defective Fas CD95 ... polyendocrine syndrome Accepted Unknown or multiple APS 1 see Addison s Disease Autoimmune progesterone ... unused data Immunology ref Autoimmune uveitis Accepted HLAB 27 ? Balo disease Balo concentric sclerosis Beh et s disease immune mediated systemic vasculitis linkage to HLA B51 HLA B27 very different manifestations with ulcers as common symptom also called Morbus Adamandiades Beh et Berger s disease ... Handbook work accessdate ref Cancer Castleman s disease Over expression of Interleukin 6 IL 6 Celiac disease Accepted ref name urlCeliac Disease cite web url http digestive.niddk.nih.gov ddiseases pubs celiac 1 title Celiac Disease format work accessdate ref ref name pmid16234635 cite journal author Meize Grochowski R title Celiac disease a multisystem autoimmune disorder journal Gastroenterol ... HLA DQ8 and DQ2.5 Chagas disease Suspected ref cite journal author Hyland KV, Engman DM title Further ... more details
Infobox disease DiseasesDB 4028 ICD10 ICD10 H 35 0 h 30 eMedicine http emedicine.medscape.com article 1225636 overview Eales disease , also known as angiopathia retinae juvenilis , periphlebitis retinae , primary perivasculitis of the retina , is an eye disease ocular disease characterized by inflammation and possible blockage of retinal blood vessels, abnormal growth of new blood vessels neovascularization , and recurrent retinal and vitreal hemorrhage s. ref name Cassin Cassin, B. and Solomon, S. Dictionary of Eye Terminology . Gainsville, Florida Triad Publishing Company, 1990. ref The condition was first described in young adult men by Henry Eales in 1880 . ref cite journal last1 Elliot first1 AJ title Recurrent Intraocular Hemorrhage in Young Adults Eales s Disease A Report of Thirty one Cases journal Transactions of the American Ophthalmological Society volume 52 pages 811 75 year 1954 pmid 13274441 pmc 1312611 ref Although men have been reported to have an increased prevalence of Eales disease, one study reported that men and women are affected equally. ref http www.emedicine.com oph topic637.htm eMedicine Eales Disease Article by Daniel B Roth Bot generated title ref Eales disease most commonly affects healthy young adults. Male predominance up to 97.6 has been reported in a majority of the series. The predominant age of onset of symptoms is between 20 and 30 years. The disease is now seen more commonly in the Indian subcontinent. Eales disease with a characteristic clinical picture, fluorescein angiographic finding , and natural course is considered a specific disease entity. Patients are often asymptomatic in the initial stages of retinal perivasculitis. Some patients may develop symptoms such as floaters, blurring vision, or even gross diminution of vision due ... with Eales disease journal Indian J Ophthalmol volume 50 issue 1 pages 35 9 year 2002 month March ... and adnexa disease stub es Enfermedad de Eales pt Enfermidade de Eales vi B nh Eales ... more details
Infobox Disease Name Fourth disease Image Caption DiseasesDB ICD10 ICD10 B 09 b 00 ICD9 ICD9 057.8 ICDO OMIM MedlinePlus eMedicineSubj eMedicineTopic MeshID Dukes disease or fourth disease is an exanthem . It is named after Clement Dukes ref C. Dukes On the confusion of two different diseases under the name of rubella rose rash . Lancet, London, 1900, 2 89 94. ref and is also known as Filatov s disease after Nil Filatov ref WhoNamedIt synd 1434 Dukes Filatov disease ref Some of these eruptions are characteristic of the causative virus, but in most cases one must be satisfied with the diagnosis of viral rash . It was never associated with a specific pathogen, ref name pmid1951267 cite journal author Morens DM, Katz AR title The fourth disease of childhood reevaluation of a nonexistent disease journal Am. J. Epidemiol. volume 134 issue 6 pages 628 40 year 1991 month September pmid 1951267 doi url http aje.oxfordjournals.org cgi pmidlookup?view long&pmid 1951267 ref and the terms fourth disease and Dukes disease are rarely used today. In 1979 Keith Powell proposed equating it with the condition currently known as Staphylococcal scalded skin syndrome . ref name pmid11214144 cite journal author Weisse ME title The fourth disease, 1900 2000 journal Lancet volume 357 issue 9252 pages 299 301 year 2001 month January pmid 11214144 doi 10.1016 S0140 6736 00 03623 0 url http linkinghub.elsevier.com retrieve pii S0140 6736 00 03623 0 ref ref name pmid367152 cite journal author Powell KR title Filatow Dukes disease. Epidermolytic toxin producing staphylococci as the etiologic agent of the fourth childhood exanthem journal Am. J. Dis. Child. volume 133 issue 1 pages 88 91 year 1979 month January pmid 367152 doi url ref Presentation Signs and symptoms may include fever , nausea , vomiting , and diarrhea , along with typical viral symptoms of photophobia , lymphadenopathy , sore throat , and possibly encephalitis . The rash may appear at any time during the illness. It is usually generalised ... more details
refimprove date November 2009 A contagious disease is a subset category of infectious disease s or communicable diseases , which are easily transmitted by physical contact hence the name origin with the person suffering the disease, or by their secretions or objects touched by them. ref http www.thefreedictionary.com Contagious disease Merriam Webster dictionary definition of contagious disease. Accessed Nov. 27, 2009 ref The non contagious category of infectious communicable diseases usually require a special mode of transmission between hosts. These include need for intermediate vector species such as a mosquito for yellow fever , direct blood contact such as transfusion or needle sharing , or sexual contact examples are AIDS and hepatitis B . The boundary between contagious and non contagious infectious diseases is not perfectly drawn, as illustrated classically by tuberculosis , which is clearly transmissible from person to person, but was not classically considered a contagious disease. In the present day, most sexually transmitted diseases are considered contagious, but only some of them are subject to medical isolation. Historical meaning Originally, the term referred to a contagion derivative of contact or disease transmissible only by direct physical contact. In the modern day, the term has sometimes been broadened to encompass any communicable or infectious disease. Often the word can only be understood in context, where it is used to emphasise very infectious, easily transmitted, or especially severe communicable disease. ref http www.encyclopedia.com doc 1O62 contagiousdisease.html ... disease. Because of the nature of non contagious communicable diseases, such as yellow fever or filariasis ... quarantine for exposed persons . Thus, a contagious disease is sometimes defined in practical ... contagious disease spread. Accessed Nov. 27, 2009. ref References reflist Medicine Category Infectious diseases Category Microbiology Disease stub fi Tartuntatauti ... more details
A polycystic disease is a disease that involves multiple cysts scattered throughout an organ, including Polycystic kidney disease Polycystic liver disease Polycystic ovary syndrome disambig ... more details
Artery disease may refer to the following coronary artery disease Peripheral artery disease, more commonly called peripheral vascular disease Carotid artery disease, more commonly called carotid artery stenosis disambig ... more details
wiktionary disease A disease is an abnormal condition of an organism that impairs bodily functions and can be deadly. Disease may also refer to Disease album Disease album , a 1993 album by G.G.F.H. Disease song Disease song , a 2002 song by Matchbox Twenty disambiguation ... more details
Infobox Disease Name Upington disease Image Caption DiseasesDB ICD10 ICD10 M 91 8 m 90 ICD9 ICD9 xxx ICDO OMIM 191520 MedlinePlus eMedicineSubj eMedicineTopic MeshID Upington disease , also called Perthes like hip disease, enchondromata and ecchondromata , ref name omim OMIM 191520 ref is an extremely rare ref RareDiseases 5421 ref autosome autosomal dominance genetics dominant ref name uad congenital disorder malformation disorder having only one published source claiming its existence on one family in three generations from South Africa . ref name uad cite journal author Schweitzer G, Jones B, Timme A title Upington disease a familial dyschondroplasia journal S. Afr. Med. J. volume 45 issue 36 pages 994&ndash 1000 year 1971 pmid 5316541 ref Characteristics The disease is characterized by Hip dysplasia human Perthes like pelvic anomalies premature closure of the capital femoral epiphyses and widened Upper extremity of femur femoral neck s with flattened femoral heads , enchondromata and ecchondromata . Genetics Image autodominant.jpg thumb right PAGENAME has an autosomal dominant pattern of inheritance. Upington disease is inherited in an autosomal dominant manner. ref name uad ref http www.orpha.net consor cgi bin OC Exp.php?Lng GB&Expert 3408 ORPHANET About rare diseases About orphan drugs Bot generated title ref This means the defective gene is located on an autosome , and one copy of the defective gene is sufficient to cause the disorder, when inherited from a parent who has the disorder. Eponym The name Upington refers to the district of Cape Province , South Africa from where the family originates. ref name omim References reflist Congenital malformations and deformations of musculoskeletal system Category Rare diseases Category Congenital disorders of musculoskeletal system Category Autosomal dominant disorders Category Genetic disorders with OMIM but no gene disease stub genetic disorder stub ... more details
Infobox Disease Name PAGENAME Image Caption DiseasesDB ICD10 ICD10 M 80 m 80 ICD10 M 90 m 86 ICD9 ICD9 730 ICD9 733 ICDO OMIM MedlinePlus eMedicineSubj eMedicineTopic MeshID D001847 Bone disease refers to the medical conditions which affect the bone . Terminology See Osteopathy A bone disease is also called an osteopathy , but because the term osteopathy is often used to a health care approach, use of the term can cause some confusion. Bone and cartilage disorders Main Osteochondrodysplasia Osteochondrodysplasia is a general term for a disorder of the development dysplasia of bone osteo and cartilage chondro . List B Bone cyst Bone spur Osteophytes Bone tumor C Craniosynostosis Coffin Lowry syndrome F Fibrodysplasia ossificans progressiva Fibrous dysplasia Fong Disease or Nail patella syndrome G Giant cell tumor of bone Greenstick Fracture H Hypophosphatasia K Klippel Feil syndrome M Metabolic Bone Disease N Nail patella syndrome O Osteoarthritis Osteitis deformans or Paget s disease of bone Osteitis fibrosa cystica or Osteitis fibrosa , or Von Recklinghausen s disease of bone Osteitis pubis Condensing osteitis or Osteitis condensans Osteitis condensans ilii Osteochondritis dissecans Osteochondroma Bone Tumor Osteogenesis Imperfecta Osteomalacia Osteomyelitis Osteopenia Osteopetrosis Osteoporosis Osteosarcoma Bone Tumor Osteonecrosis P Porotic hyperostosis Primary hyperparathyroidism R Renal Osteodystrophy S Salter Harris fractures W Water on the knee See also Osteoimmunoology External links http www.nlm.nih.gov medlineplus bonediseases.html disease stub Medical conditions Osteochondropathy Category Musculoskeletal disorders ... more details
Infobox disease Name Minor& 39 s disease ICD10 ICD9 ICD9 336.1 ICDO Image Caption OMIM MedlinePlus eMedicineSubj eMedicineTopic DiseasesDB Minor s disease , a syndrome involving the sudden onset of back pain and paralysis caused by haemorrhage into the spinal cord substance, was named after the Russia n neurologist, Lazar Salomowitch Minor 1855 1942 . The term Minor s syndrome is now only rarely used in connection with his work and is increasingly being used, both inside and outside the medical profession, to refer to superior canal dehiscence syndrome SCDS , first described in 1998 by Dr. Lloyd B. Minor of The Johns Hopkins University , Baltimore, USA. External links http www.whonamedit.com synd.cfm 1689.html whonamedit.com Minor s disease http www.whonamedit.com doctor.cfm 1619.html whonamedit.com Lazar Salomowitch Minor http www.whonamedit.com synd.cfm 1691.html whonamedit.com Minor Oppenheim syndrome http www.mercksource.com pp us cns cns hl dorlands.jspzQzpgzEzzSzppdocszSzuszSzcommonzSzdorlandszSzdorlandzSzdmd d 22zPzhtm 12304310 Dorlands Medical Dictionary Minor s disease http books.google.com books?id Elx9GJ9qrtwC&pg RA21 PA542&lpg RA21 PA542&dq 22minor s disease 22&source web&ots E3xJCwnSfw&sig 9IEA0HYcTNiCq6JugEY4as3nrqk PPA542,M1 Dictionary of Medicine French English with English French Glossary By Svetolik P. Djordjevic Minor s disease http icd9cm.chrisendres.com index.php?action search&srchtext 336.1 ICD 9 CM Classification of Diseases and Injuries Tabular Index DEFAULTSORT Minor s Disease Category Neurotrauma ... more details
Infobox disease Name Schindler disease Image Alt Caption DiseasesDB 30058 ICD10 ICD9 ICDO OMIM 609241 OMIM mult OMIM2 609242 MedlinePlus eMedicineSubj eMedicineTopic MeshID Schindler disease , also known as Kanzaki disease and Alpha N acetylgalactosaminidase deficiency is a rare Congenital disorder congenital ... R title Schindler disease the molecular lesion in the alpha N acetylgalactosaminidase gene that causes ... ref which leads to excessive Lysosomal storage disease lysosomal accumulation of glycoprotein s. ref name pmid2122119 cite journal author Cantz M, Ulrich Bott B title Disorders of glycoprotein degradation ... with this disorder. Schindler disease is an autosomal recessive disorder, meaning that one must inherit an abnormal allele from both parents in order to have the disease. There are three main types of the disease each with its own distinctive symptoms. ref name ISMRD Schindler cite web url http www.mannosidosis.org schindlerDisease.htm Pls don t change URL without checking. title Schindler disease ... problems. Infants with Schindler disease tend to die within 4 years of birth, therefore, treatment for this form of the disease is mostly palliative . However, Type II Schindler disease, with its late ... disease, but bone marrow transplants have been trialed, as they have been successful in curing other glycoprotein disorders. Amniocentesis or chorionic villus sampling can be used to screen for the disease ... can be used to diagnose Schindler disease. Genetic testing is also always an option, since different forms of Schindler disease have been mapped to the same gene on chromosome 22 ref name OMIM609241 ... forms of the disease. ref name NORD Schindler cite web url http www.rarediseases.org search rdbdetail abstract.html?disname Schindler 20Disease title Schindler Disease publisher National Organization for Rare Disorders NORD accessdate 2008 11 13 ref Schindler disease was named after Detlev Schindler M.D., the first author of a 1988 paper detailing the disease. Citation needed date November 2008 ... more details
P. last3 Norrving first3 B. editors ref Each year, heart disease kills more Americans than cancer ...Infobox disease Name Cardiovascular disease Image Cardiac amyloidosis very high mag movat.jpg Caption ... MeshID D002318 Cardiovascular disease or heart disease are a class of diseases that involve ... to any disease that affects the Circulatory system cardiovascular system as used in Medical Subject Headings MeSH C14 , it is usually used to refer to those related to atherosclerosis arterial disease ... disease range from 4 in high income countries to 42 in low income countries. More than 17 million people died from cardiovascular diseases in 2008. ref Citation title Global Atlas on cardiovascular disease ... breast cancer . ref cite web last United States authorlink Centers for Disease Control title Chronic Disease Overview publisher United States Government year 1999 ref PDAY showed vascular injury accumulates ... of coronary heart disease risk factors with the intermediate lesion of atherosclerosis in youth. The Pathobiological ... diseases. It is estimated that 82 percent of people who die of coronary heart disease ... age 55. ref Mackay, Mensah, Mendis, et al. The Atlas of Heart Disease and Stroke. World Health Organization ... elasticity and reduced arterial compliance and may subsequently lead to coronary artery disease. ref Jani B, C Rajkumar. Ageing and vascular ageing . Postgrad Med J. 2006 82 357 362. ref Gender Men are at greater risk of heart disease than pre menopausal women. ref name WHF http www.world heart federation.org cardiovascular health cardiovascular disease risk factors ref However, once past ... disease is 2 to 5 times more common in men than in women. ref name Jou99 In a study done by the World ... of coronary heart disease mortality. ref Jackson R, Chambles L, Higgins M, Kuulasmaa K, Wijnberg L, Williams D WHO MONICA Project, and ARIC Study. Sex difference in ischaemic heart disease mortality ... in cardiovascular disease is hormonal difference. ref name Jou99 Among women, estrogen is the predominant ... more details
name Karim cite journal author Karim B title Caroli s Disease Case Reports journal Indian Pediatrics ...Infobox disease Name Caroli disease Image BiliaryTract.gif Caption Figure 1 Bilary tract, system, or tree ... disease is a rare inherited disorder characterized by dilatation of the intrahepatic bile ducts. There are two types of Caroli disease, the most common being the simple, or isolated case where the bile ... been discovered. Caroli disease is also associated with liver failure and polycystic kidney disease . The disease affects about 1 in 1,000,000 people, with more reported cases of Caroli syndrome than of Caroli disease. ref name EMedRad EMedicine radio 131 Romano WJ Caroli Disease ref Caroli disease ... biliary tree . Caroli disease is distinct from other diseases that cause ductal dilatation caused ... life threatening hepatobiliary disease. ref cite journal author Miller WJ, Sechtin AG, Campbell WL, Pieters PC title Imaging findings in Caroli s disease journal AJR Am J Roentgenol volume 165 issue 2 ... library topics volume iv 1 c CAROLIS DISEASE.aspx Caroli s Disease Gastrointestinal Imaging. 2008. Medcyclopaedia , 4 1 ref Caroli disease usually occurs in the presence of other diseases, such as autosomal recessive polycystic kidney disease , cholangitis , gallstones , bilary abscess ... Karim People with Caroli disease are 100 times more at risk for cholangiocarcinoma than the general population. ref name Medcyc After recognizing symptoms of related diseases, Caroli disease can be diagnosed ... AN, Saeian K title Caroli s disease identification and treatment strategy journal Curr Gastroenterol ... ref Commonly the disease is limited to the left lobe of the liver. Images taken by CT scan , X ray , or MRI ... , tubular dilation of the bile ducts can be seen. On a CT Scan, Caroli disease can be observed by noting ... streak. ref name Chiba Caroli disease is commonly diagnosed after this central dot sign is detected ... N, Fujimoto H, Kondo F title Caroli s disease central dot sign re examined by CT arteriography ... more details
cleanup linkrot date August 2011 Infobox album See Wikipedia WikiProject Albums Name A Diamond for Disease Type ep Artist Arsis Cover Arsis A Diamond for Disease.jpg Alt Released October 25, 2005 Recorded Hairy Breakfast Productions br Max Trax Studios Genre Melodic death metal br Technical death metal Length 19 57 Label Willowtip Records Producer Eyal Levi br Brett Portzer Reviews Exclaim favorable ref http www.exclaim.ca musicreviews generalreview.aspx?csid2 846&fid1 19461&csid1 76 ref Stylus Magazine B ref http www.stylusmagazine.com reviews arsis neuraxis a diamond for disease trilateral progression.htm ref Last album A Celebration of Guilt br 2004 This album A Diamond for Disease br 2005 Next album United in Regret br 2006 A Diamond for Disease is an Extended play EP by Arsis band Arsis released on October 25, 2005 via Willowtip Records . The title track, A Diamond for Disease , took almost four months to write. This release also includes an Alice Cooper cover from the Raise Your Fist and Yell album showing the band members love of classic heavy metal music heavy metal , and The Promise of Never which is a re recorded track from the band s 2001 demo, originally titled Fortune s Envy . The EP was mastered by James Murphy metal guitarist James Murphy , who is best known for his work with Death metal band Death , Testament band Testament , Obituary band Obituary , and Disincarnate . Track listing tracklist writing credits yes title1 A Diamond for Disease writer1 James Malone length1 12 52 title2 Raise Your Fist and Yell Roses on White Lace note2 Alice Cooper cover writer2 Alice Cooper , Kane Roberts length2 4 17 title3 The Promise of Never writer3 James Malone length3 2 50 Personnel James Malone guitar, bass, and vocals Mike Van Dyne drums References Reflist DEFAULTSORT Diamond for Disease, A Category 2005 EPs Category Arsis albums 2000s death metal album stub ... more details
Infobox Disease Name Sandhoff disease Image Caption DiseasesDB 29469 ICD10 ICD10 E 75 0 e 70 ICD9 ICD9 330.1 ICDO OMIM 268800 MedlinePlus eMedicineSubj eMedicineTopic MeshID D012497 Sandhoff disease , also known as Sandhoff Jatzkewitz disease , variant 0 of GM2 Gangliosidosis or Hexosaminidase A and B ... 9 year 2004 doi 10.1023 B BOLI.0000028777.38551.5a pmid 15159655 ref Adult onset form of the disease ... functional beta hexosaminidases A and B ref name KS cite journal pmid 5651108 year 1968 month ... case of Tay Sachs disease with additional storage of kidney globoside in visceral organs volume ... pattern in Tay Sachs disease volume 4 issue 4 pages 351 354 journal FEBS Lett doi 10.1016 0014 ... 1189 91 journal Klin Wochenschr ref ref name omim OMIM 268800 Sandhoff Disease ref neurodegenerative disorder is clinically almost indistinguishable from Tay Sachs disease , another genetic disorder that disrupts beta hexosaminidases A and S. There are three subsets of Sandhoff disease based on when first symptoms appear classic infantile, juvenile and adult late onset. History Sandhoff disease is one of several forms of what was formerly known as amaurotic idiocy. This inherited disease is characterized ... Acta ref , Sandhoff disease in 1968 ref name KS , Tay Sachs Disease ref name KS2 ref cite journal pmid 5793973 year 1969 month August author Okada S, O Brien JS title Tay Sachs disease generalized ... disease, when Konrad Sandhoff studied the biochemistry of sphingolipids and gangliosides in the laboratory ... disease studied so far, globoside accumulated in the visceral organs and, most importantly, hexosaminidase activity was almost completely absent. The disease causing catabolic enzyme deficiency of hexosaminidases ... organs and published in 1968 ref name KS . Types There are three different types of Sandhoff disease ... title Impact of premature stop codons on mRNA levels in infantile Sandhoff disease volume 3 ... infantile form of the disease is classified by the development of symptoms anywhere from 2 months ... more details
Hemophilia Hemophilia A Hemophilia B also known as Christmas disease Hemophilia C Von Willebrand disease ...Infobox Disease Name PAGENAME Image Caption DiseasesDB ICD10 ICD9 ICDO OMIM MedlinePlus eMedicineSubj eMedicineTopic MeshID D006402 Hematologic diseases are disorders which primarily affect the blood. Myeloid Hemoglobinopathy Hemoglobinopathies congenital abnormality of the hemoglobin molecule or of the rate of hemoglobin synthesis Sickle cell disease Thalassemia Methemoglobinemia Anemia s lack of red blood cells or hemoglobin Iron deficiency anemia Megaloblastic anemia Vitamin B12 Vitamin B small sub 12 sub small deficiency Pernicious anemia Folate deficiency Hemolytic anemias destruction of red blood cells Genetic disorders of RBC membrane Hereditary spherocytosis Hereditary elliptocytosis Congenital dyserythropoietic anemia Genetic disorders of RBC metabolism Glucose 6 phosphate dehydrogenase deficiency G6PD Pyruvate kinase deficiency Immune mediated hemolytic anemia Coombs test Direct Coombs test direct Coombs test is positive Autoimmune hemolytic anemia Warm antibody autoimmune hemolytic ... antibodies Cold agglutinin disease Cold antibody autoimmune hemolytic anemia Idiopathic cold ... anemia Hemolytic disease of the newborn HDN Rh disease Rh D ABO hemolytic disease of the newborn Anti Kell hemolytic disease of the newborn Rhesus c hemolytic disease of the newborn Hemolytic disease of the newborn anti RhE Rhesus E hemolytic disease of the newborn Other blood group incompatibility ... Hematological malignancies Lymphoma s Hodgkin s disease Non Hodgkin s lymphoma includes the next ... leukemia CML T cell prolymphocytic leukemia T PLL B cell prolymphocytic leukemia B PLL Chronic ... disease Monoclonal gammopathy of undetermined significance Hemophagocytic lymphohistiocytosis Hematological changes secondary to non hematological disorders Anemia of chronic disease Infectious mononucleosis ... Diseases of RBCs and megakaryocytes Monocyte and granulocyte disease Certain conditions originating ... more details
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