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...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2024-03-01
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Series: | Otolaryngology Case Reports |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2468548823000681 |