Wardenburg syndrome type 2 in a woman with no genomic mutation commonly associated with the syndrome
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Audrey Rutherford, Donald A Glass Ii1, Nnenna G Agim
1Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, Texas, McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, Texas.. donald.glass@utsouthwestern.edu.
Abstract:
Waardenburg Syndrome (WS) is a condition characterized by pigmentary changes of the hair or skin, hearing loss, heterochromia iridis, and dystopia canthorum. There are four main types of WS, which can be commonly caused by mutations in the PAX3, MITF, EDNRB, EDN3, SNAI2, or SOX10 genes. Herein, we present a patient with Waardenburg Syndrome type 2 with no findings of mutations in the commonly associated genes.
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