A de novo SOX10 mutation causing severe type 4 Waardenburg syndrome without Hirschsprung disease

✍ Scribed by Yves Sznajer; Cristina Coldéa; Françoise Meire; Isabelle Delpierre; Tayeb Sekhara; Renaud L. Touraine

• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 109 KB
• Volume: 146A
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.32247

✦ Synopsis

Abstract

Type 4 Waardenburg syndrome represents a well define entity caused by neural crest derivatives anomalies (melanocytes, intrinsic ganglion cells, central, autonomous and peripheral nervous systems) leading, with variable expressivity, to pigmentary anomalies, deafness, mental retardation, peripheral neuropathy, and Hirschsprung disease. Autosomal dominant mode of inheritance is prevalent when Sox10 gene mutation is identified. We report the natural history of a child who presented with synophrys, vivid blue eye, deafness, bilateral complete semicircular canals agenesis with mental retardation, subtle signs for peripheral neuropathy and lack of Hirschsprung disease. SOX10 gene sequencing identified “de novo” splice site mutation (c.698‐2A > C). The present phenotype and the genotype findings underline the wide spectrum of SOX10 gene implication in unusual type 4 Waardenburg syndrome patient. © 2008 Wiley‐Liss, Inc.