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{{disease|F45.3|Da Costa´s syndrome|''ICD 10 classification'}} == Da Costa’s Syndrome == ...

...l affected persons experience all the symptoms associated with the greater syndrome. Fibromyalgia is considered a controversial diagnosis by some authors who c ...sketal symptoms and non-REM sleep disturbance in patients with "fibrositis syndrome" and healthy subjects", ''Psychosom Med'' 37(4):341-51, pmid=169541</ref> S ...

...l.'' |title=Failure to detect the novel retrovirus XMRV in chronic fatigue syndrome |journal=PLoS ONE |volume=5 |issue=1 |pages=e8519 |year=2010 |pmid=20066031 ...in cancerous prostate tissues using a [[microarray]] containing samples of genetic material from about 950 viruses. The screen indicated the presence of a gam ...

It is difficult to distinguish between genetic and cryptogenic syndromes. ...cbi.nlm.nih.gov/pubmed/28993753 Electroencephalography in the Diagnosis of Genetic Generalized Epilepsy Syndromes] ...

Angelman syndrome is a genetic disorder, associated with [[epilepsy|convulsions]]. On 1965, Dr [[Harry Ang *[http://ghr.nlm.nih.gov/condition/angelman-syndrome] ...

...y been observed in girls or in boys with [[Harry Klinefelter|Klinefelter]] syndrome. ...to Shah et al 2009 the most reliable feature of [[Jean Aicardi|Aicardi]]'s syndrome is chorioretinal lacunae<ref>The encyclopaedia of neuropsychological disord ...

preferably [[Harry F.Klinefelter|Klinefelter]]-Reifenstein-Albright syndrome.<ref>Pschyrembel Klinisches Wörterbuch 256.Auflage S.857</ref> Klinefelter syndrome, 47,XXY (KS), occurs in about 150 per 100,000 males and is the most frequen ...

...7-9856-2013-14.pdf Endocrine manifestations and management of Prader-Willi syndrome]</ref>. It was first described in 1956 by [[Andrea Prader]] (1919–2001), He [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510909/ Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromoso ...

...tomatic of a hidden histopathological or cellular alteration, but not of a genetic nature<ref>http://www.cun.es/diccionario-medico/terminos/epilepsia-criptoge *genetic e.g. [[Dravet%27s_syndrome|Dravet syndrome]] ...

{{disease|Q87.1|Cornelia de Lange Syndrome}} ...al, cognitive and medical challenges and affects both genders equally. The syndrome is named after Dutch pediatrician [[Cornelia de Lange|Cornelia Catharina de ...

...rt's syndrome|GS]], also called Gilbert–Meulengracht syndrome, is a common genetic liver disorder found in 3-12% of the population. {{disease|E80.4|Gilbert's syndrome}} ...

...t The Kurume Med. J. 1986]</ref> (''Kleeblattschädel'' syndrome) is a rare genetic disease, a deformity is etiologically and pathologically heterogeneous, so ...

...me 22<ref>Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology</ref> , about 44% of people develops [[epilepsy|seizures]] ...ion in Autism Spectrum Disorders and Shankopathies Such as Phelan McDermid Syndrome] ...