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A 22q13.1 duplication in mosaicism including SOX10
William Bertani-Torres1,2, Margaux Serey-Gaut3,4, Judite de Oliveira3
1Université Paris Cité, Paris, France.
American Journal of Medical Genetics. Part A
|August 3, 2023
Summary
This study details a rare case of Waardenburg syndrome (WS) caused by a mosaic duplication in chromosome 22q13.1. The findings expand understanding of SOX10 gene duplications and their associated developmental impacts.
Area of Science:
- Genetics
- Medical Science
- Developmental Biology
Background:
- Waardenburg syndrome (WS) is a genetic disorder characterized by hearing loss and pigmentation anomalies.
- WS Type 2 (WS2) lacks distinct features, complicating diagnosis.
- SOX10 gene mutations are implicated in various WS types, but duplications are less understood.
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