Williams syndrome is a rare genetic disorder resulting in prenatal and postnatal development problems, growth disorders, and characteristic facial features. |
Williams syndrome (WS) is a genetic condition that is present at birth and can affect anyone. It is characterized by medical problems, ... |
Williams Syndrome is a chromosome disorder where she has a micro-deletion on chromosome 7. For our daughter it was a total fluke in nature. 1 in 20000 at the ... |
Facial features frequently include a broad forehead, underdeveloped chin, short nose, and full cheeks. Mild to moderate intellectual disability is observed, ... Gabrielle Marion-Rivard · Supravalvular aortic stenosis · Syndromic autism |
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