williams syndrome
Williams Syndrome Information Page: National Institute of Neurological …
Williams syndrome information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
Clinical Summaries [Clinical Summaries]
Congenital long-QT syndrome is a type of heritable primary cardiac arrhythmia susceptibility disease and a known cause of sudden death, especially in young adults and children.
Williams Syndrome Association
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Williams syndrome - Wikipedia, the free encyclopedia
Williams syndrome (WS; also Williams-Beuren syndrome or WBS) is a rare neurodevelopmental disorder caused by a deletion of about 26 genes from the long arm of chromosome 7. [1]
Yale Researchers Awarded Grant To Develop Treatment Of Williams Syndrome
Main Category: Cardiovascular / Cardiology Also Included In: Pediatrics / Children’s Health Genetics Yale researchers have been awarded a $320,000 grant from The Kiev Foundation to study new ways to treat Williams Syndrome, a rare, thus far incurable chromosomal disorder that causes cardiovascular and connective tissue problems.
What is Williams syndrome
Williams syndrome is a rare genetic condition (estimated to occur in 1/10,000 births) which causes medical and developmental problems. Williams syndrome was first recognized as a …
The distinct cognitive syndromes of Parkinson’s disease: 5 year follow-up of the CamPaIGN cohort
Factors influencing their evolution remain unclear but are crucial to the development of targeted therapeutic strategies.
