Co-Occurrence of a De Novo Williams and 22q11.2 Microdeletion Syndromes

摘要

We report on a child with de novo deletions involving the 7q11.23 (Williams syndrome) and 22q11.2 (Velocardiofacial/DiGeorge syndrome) regions. We describe the clinical features of this rare double microdeletion syndrome reported here for the first time. (C) 2015 Wiley Periodicals, Inc.