Erschienen in:
15.06.2016 | Scientific Letter
Williams-Beuren Syndrome with Mirror Movements
verfasst von:
Sedat Işıkay, Sadettin Sezer, Serkan Kırık, Olcay Güngör
Erschienen in:
Indian Journal of Pediatrics
|
Ausgabe 12-13/2016
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Excerpt
To the Editor: Williams-Beuren Syndrome (WBS) is a rare neurodevelopmental disorder caused by deletion of chromosome 7 at q11.23. It is characterized by distinctive facies, congenital cardiovascular malformations, intellectual disabilities, and various other manifestations [
1,
2]. Here, we present a child with WBS who presented with abnormal involuntary hand movements. …