Barakat syndrome presenting as isolated sensorineural hearing loss

Barakat syndrome is a rare autosomal dominant disease caused by haplo-insufficiency of transcription factor GATA3 on chromosome 10p14. It is characterized by a triad of hypoparathyroidism, sensorineural hearing loss, and renal disease with high phenotypic heterogeneity. Here we report a case of Bara...

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Bibliographic Details
Main Authors: Angela S. Zhu, Danielle Reny Larrow, Michael S. Cohen
Format: Article
Language:English
Published: Elsevier 2024-03-01
Series:Otolaryngology Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2468548823000681