759.89 ICDO OMIM 117550 MedlinePlus eMedicineSubj eMedicineTopic Sotossyndrome cerebral gigantism ... muscle tone , and speech impairments. Children with Sotossyndrome tend to be large at birth and are often ... may also occur. Although most cases of Sotossyndrome occur sporadically, familial cases have also been reported. It is similar to Weaver syndrome . Epidemiology Incidence is approximately ... head. Adult height is usually in the normal range, however. People with Sotossyndrome often have .... Other signs of Sotossyndrome include an abnormal side to side curvature of the spine scoliosis ... people with Sotossyndrome have developed cancer, most often in childhood, but no single form of cancer has been associated with this condition. It remains uncertain whether Sotossyndrome increases ... gene cause Sotossyndrome. ref name pmid15720303 cite journal author Melchior L, Schwartz M ... 100 Sotossyndrome mutations journal Ann. Hum. Genet. volume 69 issue Pt 2 pages 222 6 year 2005 month ... change leading to Sotossyndrome deletes genetic material from the region of chromosome 5 containing ..., overgrowth, and the other features of Sotossyndrome. About 95 percent of Sotossyndrome ... family member. These cases helped researchers determine that Sotossyndrome has an autosomal dominant ... cell is sufficient to cause the disorder. Treatment There is no standard course of treatment for Sotossyndrome. Treatment is symptomatic. Prognosis Sotossyndrome is not a life threatening disorder and patients may have a normal life expectancy. The initial abnormalities of Sotossyndrome usually ... also Perlman syndrome Beckwith Wiedemann syndrome References reflist External links http www.orpha.net ... sotos Phakomatoses and other congenital malformations not elsewhere classified Category Syndromes Link GA pl de Sotos Syndrom es S ndrome de Sotos fr Syndrome de Sotos it Sindrome di Sotos nl Syndroom van Sotos pl Zesp Sotosa pt S ndrome de Sotos ru fi Sotosin oireyhtym ... more details
Peter Sotos born April 17, 1960 is a Chicago born writer and musician. cn date December 2011 Musical career Until 2003 he was a member of the seminal List of post industrial music genres and related fusion genres Power electronics power electronics group Whitehouse band Whitehouse . cn date December 2011 Works Pure Self published and released two issues, with a third having been completed before controversy of publication led to now infamous trial. Parasite Self published twenty issues. Total Abuse Collected Writings, 1984 1995 Pure, Tool, Parasite , 1995 Goad to Hell Enterprises, Portland, OR, ISBN ... Void Books . Proxy Peter Sotos Pornography 1991 2000 , 2005 Creation Books , a compendium of five of Sotos works Tool , Special , Tick , Index and Lazy . First edition, with CD by Sotos and Steve Albini ... Peter Sotos Volume One , 2009 Creation Books Waitress , 2009 Creation Books Third in a series .... Public The Collected Peter Sotos Volume Two , 2009 Creation Books Waitress , 2009 Creation Books Fourth ... of Public. Private The Collected Peter Sotos Volume Three , 2009 Creation Books Waitress , 2009 Creation ... with pre orders of Private. Kept The Collected Peter Sotos Volume Four , 2010 Creation Books Texts featuring Sotos Apocalypse Culture , edited by Adam Parfrey , interview with Sotos Amok Books, 1990, ISBN 0 922915 05 9 .45 Dangerous Minds edited by Steve Blush and George Petros , interview with Sotos ... by Sotos Feral House , 2000, ISBN 0 922915 57 1 The Gates of Janus by Ian Brady , afterword by Sotos ... King, contributed to by Sotos Creation Books, 2003, ISBN 1 84068 090 3 . External links http www.creationbooks.com ... Sotos A Case Study in Lust and the Unconditioned by Michael Lujan http nypress.com 18 29 books travisjeppesen.cfm ... Sotos, Peter ALTERNATIVE NAMES SHORT DESCRIPTION DATE OF BIRTH April 17, 1960 PLACE OF BIRTH DATE OF DEATH PLACE OF DEATH DEFAULTSORT Sotos, Peter Category 1960 births Category Living people Category ... Category School of the Art Institute of Chicago alumni fr Peter Sotos ... more details
Jim Sotos was a film director in the 1970s and 80s. He directed the 1975 in film 1975 film , Forced Entry 1975 film Forced Entry the 1983 in film 1983 film , Sweet Sixteen 1983 film Sweet Sixteen the 1985 in film 1985 film , Hot Moves and the 1989 in film 1989 film , Beverly Hills Brats . He was also a producer and filmographer on other films. External links imdb name id 0815634 Persondata Metadata see Wikipedia Persondata . NAME Sotos, Jim ALTERNATIVE NAMES SHORT DESCRIPTION DATE OF BIRTH PLACE OF BIRTH DATE OF DEATH PLACE OF DEATH DEFAULTSORT Sotos, Jim Category Year of birth missing living people Category Living people Category American film directors Category Place of birth missing living people film director stub ... more details
File Greenwich Island location map.png thumb Location of Greenwich Island in the South Shetland Islands. Sotos Point is a glaciated point projecting 180 m into the southeast part of Discovery Bay Antarctica Discovery Bay , Greenwich Island South Shetland Islands Greenwich Island in the South Shetland Islands , Antarctica and forming the east side of the entrance to Montecinos Cove coord 62 29 57 S 59 40 59 W . Sotos Point was named by the 1949 50 Chilean Antarctic Expedition after several members of the expedition with the surname Soto, while Montecinos Cove was named by the 1947 Chilean Antarctic Expedition after a member of the expedition. Location The point is located at coord 62 29 46.6 S 59 40 28 W which is 3.3 km south by west of Ash Point and 1.18 km east northeast of Ferrer Point Chilean mapping in 1951, British in 1968, and Bulgarian in 2005 and 2009 . Maps L.L. Ivanov et al. commons Image Livingston Greenwich map.jpg Antarctica Livingston Island and Greenwich Island, South Shetland Islands . Scale 1 100000 topographic map. Sofia Antarctic Place names Commission of Bulgaria, 2005. L.L. Ivanov. http id team.org apc Apcbg Web New files image023.jpg Antarctica Livingston Island and Greenwich, Robert, Snow and Smith Islands . Scale 1 120000 topographic map. Troyan Manfred W rner Foundation, 2009. ISBN 978 954 92032 6 4 Reference http data.aad.gov.au aadc gaz scar SCAR Composite Antarctic Gazetteer . Category Headlands of Greenwich Island SouthShetlandIslands geo stub ... more details
Other uses In medicine and psychology , a syndrome is the association of several clinically recognizable features, sign medicine signs observed by someone other than the patient , symptom s reported by the patient ... in association. Some syndromes, such as Down syndrome , have only one cause others, such as Parkinsonian syndrome , have multiple possible causes. In other cases, the cause of the syndrome is unknown. The term syndrome derives from the Greek language Greek sundrom and means concurrence of symptoms ..., A Greek English Lexicon , on Perseus ref A familiar syndrome name often continues to be used even ... severe than a defined syndrome, but that nevertheless can be identified and related to the full blown syndrome. A culture bound syndrome is a set of symptoms where there is no evidence of an underlying ... and associated conditions The description of a syndrome usually includes a number of essential characteristics ... and minor findings typical of the syndrome, there may be an association with other conditions, meaning that in persons with the specified syndrome these associated conditions occur more frequently than would be expected by chance. While the syndrome and the associated conditions may be correlation .... An example would be Down syndrome , which has the associated condition of diabetes mellitus ... of the syndrome. Examples One recent case study is AIDS acquired immune deficiency syndrome ..., finally explaining the hitherto mysterious syndrome . Severe acute respiratory syndrome SARS severe acute respiratory syndrome is an even more recent example of a syndrome in medicine that was later ..., 980 1037 , in The Canon of Medicine , pioneered the idea of a syndrome in the diagnosis of specific ... 0 19 513580 6. ref Verify source date September 2010 The concept of a medical syndrome was further ... Toxidrome Withdrawal Withdrawal syndrome References Reflist External links Wiktionary syndrome ... ca S ndrome cs Syndrom de Syndrom et S ndroom es S ndrome eo Simptomaro eu Sindrome fa fr Syndrome ... more details
Overgrowth syndrome is a group of genetic disorders in which there is an abnormal increase in the size of the body or a body part that is often noted at birth . Examples of overgrowth syndromes include neurofibromatosis , Sotossyndrome , Beckwith Wiedemann syndrome , Simpson Golabi Behmel syndrome , Weaver syndrome , Proteus syndrome , Sturge Weber syndrome , and fragile X syndrome . Many of these syndromes increase the risk of cancer . See also Gigantism External links http www.cancer.gov Templates db alpha.aspx?CdrID 367429 Overgrowth syndrome entry in the public domain NCI Dictionary of Cancer Terms http bigheaded.org Macrocephalia is the is a condition in which there is an abnormally overgrown brain. NCI cancer dict Multiple abnormalities Category Growth disorders Category Human height Category Growth hormones Category Neuroendocrinology Category People with gigantism Category Size oncology stub ... more details
of Perlman syndrome also overlap with other disorders associated with Wilms tumor namely Sotossyndrome ...Infobox disease Name Perlman syndrome Image Caption DiseasesDB ICD10 C64 ICD9 ICDO OMIM 267000 MedlinePlus eMedicineSubj eMedicineTopic MeshName MeshNumber Perlman syndrome PS also called renal hamartomas , nephroblastomatosis and fetal gigantism is a rare overgrowth syndrome overgrowth disorder present ... at an early age. The prognosis for Perlman syndrome is severe and associated with a high neonatal mortality . Signs and symptoms Perlman syndrome is an uncommon genetic disorder grouped with overgrowth syndrome in which an abnormal increase is often noted at birth in the size of the body or a body ... cite journal author Perlman M title Perlman syndrome familial renal dysplasia with Wilms ... syndrome is a rare disease with an estimated incidence of less than 1 in 1,000,000. As of 2008 ... url http www.orpha.net consor cgi bin OC Exp.php?Lng GB&Expert 2849 title Perlman syndrome accessdate ... syndrome has an autosomal recessive pattern of inheritance. The genetic basis of the syndrome is unknown ..., the sex ratio of male to female is 2 1. The syndrome has been described in both consanguineous and non consanguineous couplings. ref name Piccione cite journal title Perlman syndrome renal hamartomas ... A case of Perlman syndrome associated with a cytogenetic abnormality of chromosome 11 abstract journal ... The diagnosis of Perlman syndrome is based on observed phenotypic features and confirmed by histological ... for Perlman syndrome although there is no conclusive laboratory test to confirm the diagnosis ... be the first signs of Perlman. ref name Piccione Using ultrasound diagnosis, Perlman syndrome has been detected at 18 weeks. During the first trimester , the common abnormalities of the syndrome observed ... Piccione ref name Emery Differential diagnosis Perlman syndrome shares clinical overlaps with other overgrowth disorders with similarities to Beckwith Wiedemann syndrome and Simpson Golabi Behmel syndrome ... more details
Infobox disease Name Weaver syndrome of the face Image Caption DiseasesDB ICD10 ICD10 Q 87 3 q 80 ICD9 ICDO OMIM 277590 MedlinePlus eMedicineSubj eMedicineTopic MeshID Weaver syndrome also called Weaver Williams syndrome is a congenital disorder associated with rapid growth beginning in the prenatal period, a characteristic facial appearance and certain skeletal features. It was first described by Weaver in 1974. ref cite journal author Weaver DD, Graham CB, Thomas IT, Smith DW title A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and al J. Pediatr. volume 84 issue 4 pages 547 52 year 1974 pmid 4366187 doi 10.1016 S0022 3476 74 80675 X journal The Journal of Pediatrics ref It can be associated with NSD1 . ref cite journal author Douglas J, Hanks S, Temple IK, et al. title NSD1 mutations are the major cause of Sotossyndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes journal Am. J. Hum. Genet. volume 72 issue 1 pages 132 43 year 2003 pmid 12464997 doi 10.1086 345647 pmc 378618 ref A second gene EZH2 Histone lysine N methyltransferase has also been associated with this disease. ref name Tatton Brown2011 Tatton Brown K, Hanks S, Ruark E, Zachariou A, Duarte SD, Ramsay E, Snape K, Murray A, Perdeaux ER, Seal S, Loveday C, Banka S, Clericuzio C, Flinter F, Magee A, McConnell V, Patton M, Raith W, Rankin J, Splitt M, Strenger V, Taylor C, Wheeler P, Temple IK, Cole T, Childhood Overgrowth Collaboration T, Douglas J, Rahman N 2011 Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height. Oncotarget ref EZH2 Mutations in EZH2 cause Weaver Syndrome . ref cite journal quotes yes last Gibson first William T authorlink coauthors Hood Rebecca L, Zhan Shing Hei, Bulman Dennis E .... title Mutations in EZH2 Cause Weaver Syndrome journal American journal of human genetics volume issue ... See also Perlman syndrome Beckwith Wiedemann syndrome References reflist Phakomatoses and other congenital ... more details
wiktionarypar SyndromeSyndrome may refer to Syndrome in medicine Syndrome decoding , in coding theory Syndrome The Incredibles , a fictional character Syndrome video game series disambig fr Syndrome homonymie ko it Sindrome disambigua nl Syndrome ja ru ... more details
Bouveret syndrome can refer to Bouveret Hoffmann syndrome, or paroxysmal tachycardia Bouveret s syndrome, or gastric outlet obstruction due to a gallstone disambig ... more details
The Immunity Syndrome may refer to The Immunity Syndrome Space 1999 The Immunity Syndrome Space 1999 , a 1977 episode of Space 1999 The Immunity Syndrome Star Trek The Immunity Syndrome Star Trek , a 1968 second season episode of Star Trek The Original Series disambiguation ... more details
Steal syndrome may refer to Cardiac steal syndrome Subclavian steal syndrome , often associated with fainting, and typically due to atherosclerosis Vascular access steal syndrome , a problem related to a surgically created vascular access fistula for hemodialysis See also Steele Richardson Olszewski syndrome, alternative name for progressive supranuclear palsy Disambig ... more details
Syndrome X may refer to Cardiac syndrome X Metabolic syndrome Single X syndrome, where an individual has a single X chromosome, typically described as Turner syndrome The otherwise unidentifiable rare disease afflicting Brooke Greenberg . disambiguation ... more details
Meadow s syndrome or Meadows syndrome can refer to Munchausen syndrome by proxy , named for Roy Meadow , who characterized it in 1977 Postpartum cardiomyopathy , named for William Meadows , who characterized it in 1957 disambig ... more details
Bazex syndrome may refer to Bazex Dupr Christol syndrome Acrokeratosis paraneoplastica of Bazex disambig Category Conditions of the skin appendages Category Genodermatoses ... more details
Pilotto syndrome is a rare syndrome which affects the face , heart , and back . The syndrome can cause a cleft lip and palate , scoliosis , and mental retardation . The Office of Rare Diseases and National Institutes of Health have classified this syndrome as affecting less than 200,000 people in the United States . ref cite web url http wrongdiagnosis.com p pilotto syndrome intro.htm title Pilotto syndrome publisher Health Grades Inc. accessdate 17 February 2010 ref References reflist disease stub Category Congenital disorders Category Syndromes Category Rare diseases ... more details
HEC syndrome is a syndrome characterized by hydrocephalus , endocardial fibroelastosis and cataract s. References cite journal author Devi A, Eisenfeld L, Uphoff D, Greenstein R title New syndrome of hydrocephalus, endocardial fibroelastosis, and cataracts HEC syndrome . journal Am J Med Genet volume 56 issue 1 pages 62 6 year 1995 pmid 7747788 doi 10.1002 ajmg.1320560114 External links OMIM 600559 disease stub Category Syndromes ... more details
Expert subject Medicine date March 2009 FACES syndrome is a syndrome of unique facial features, Anorexia symptom anorexia , cachexia , Human eye eye and Human skin skin anomalies. ref name pmid6438152 cite journal author Friedman E, Goodman RM title The FACES syndrome a new syndrome with unique facies, anorexia, cachexia, and eye and skin lesions journal J. Craniofac. Genet. Dev. Biol. volume 4 issue 3 pages 227 31 year 1984 pmid 6438152 ref References reflist disease stub Category Syndromes Category Musculoskeletal disorders Category Rare diseases roa rup Faces syndrome ... more details
Infobox disease Name Aicardi syndrome ICD10 ICD10 G 93.8 g 93 ICD9 ICD9 742.2 ICDO Image Caption OMIM 304050 OMIM mult MedlinePlus 001664 eMedicineSubj ped eMedicineTopic 58 DiseasesDB 29761 Aicardi syndrome is a rare genetic congenital disorder malformation syndrome characterized by the partial or complete ... syndrome is theorized to be caused by a defect on the X chromosome as it has thus far only been observed in girls or in boys with Klinefelter s syndrome . Confirmation of this theory awaits the discovery of the gene which causes Aicardi syndrome. Symptoms typically appear before a baby reaches about ... syndrome in 1965 by Jean Aicardi , a French neurologist. A review article by Dr. Aicardi Aicardi J, Aicardi syndrome old and new findings, Int Pediatr. 1998 14 1 5 8 describes the syndrome. Aicardi syndrome should not be confused with Aicardi Gouti res syndrome , a distinct disorder. Citation needed date July 2008 Epidemiology Worldwide prevalence of Aicardi Syndrome is estimated at several ... cases of Aicardi syndrome have been in females. The few males that have been identified with Aicardi syndrome have proved to have 47 chromosomes including an XXY sex chromosome complement, a condition called Klinefelter syndrome . Citation needed date July 2008 Aicardi syndrome appears to be lethal in normal males who have only one X chromosome and a Y chromosome . In other words, Aicardi syndrome ... that is lethal in XY males. Citation needed date July 2008 All cases of Aicardi syndrome are thought to be due to new mutations . No person with Aicardi syndrome is known to have transmitted the X linked gene responsible for the syndrome to the next generation. Features Children are most commonly identified with Aicardi syndrome before the age of five months. A significant number of girls are products ... July 2008 Diagnosis Aicardi syndrome is typically characterized by the following triad of features however, one of the classic features being missing does not preclude a diagnosis of Aicardi Syndrome ... more details
Wikify date December 2010 expert subject Genetics date August 2008 Infobox disease Name Hydrolethalus syndrome Image Alt Caption DiseasesDB 34380 ICD10 ICD9 ICDO OMIM 236680 MedlinePlus eMedicineSubj eMedicineTopic MeshID GeneReviewsID GeneReviewsName Hydrolethalus syndrome less commonly referred to as Salonen Herva Norio syndrome is a rare genetic disorder that causes improper fetal development, resulting in birth defects and often stillbirth . ref http www.enotes.com genetic disorders encyclopedia hydrolethalus syndrome ref It is associated with HYLS1 mutations. Symptoms Hydrolethalus syndrome can cause heart and brain defects, a cleft lip or palate, an abnormally shaped nose or jaw, or incomplete lung development. These defects are typically serious enough to cause stillbirth or death within a few days of birth. References reflist DEFAULTSORT Hydrolethalus Syndrome Category Congenital disorders disease stub ... more details
Unreferenced stub auto yes date December 2009 Psychoorganic syndrome is a progressive disease comparable to presenile dementia . It is caused by exposure to organic solvents such as toluene . See also Neurotoxicity Category Neurological disorders DEFAULTSORT Psychoorganic Syndrome Psych stub Disease stub pl Zaburzenia psychoorganiczne ... more details
Unreferenced stub auto yes date December 2009 Orphan date February 2009 In medicine, Valentino s syndrome is pain presenting in the right lower quadrant of the abdomen caused by a duodenum duodenal peptic ulcer ulcer with perforation through the retroperitoneum . DEFAULTSORT Valentino s Syndrome Med stub Category Abdominal pain ... more details
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