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January 1, 2019Practica Oto-Rhino-Laryngologica

Auditory Evaluation in a Patient with HDR Syndrome

Haruki Kondo Hiroshi Nakanishi Katsuyoshi SUZUKI Katsura Hakamada Seiji Hosokawa Hiroyuki Mineta Jun Okamura

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Abstract

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HDR syndrome is an autosomal dominant disorder characterized by hypoparathyroidism, sensorineural deafness, and renal dysplasia. Herein, we present a case of HDR syndrome caused by a GATA3 mutation.

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Kondo et al. (2019) studied this question.

synapsesocial.com/papers/6a9a816a8e341895a89c66e2 https://doi.org/10.5631/jibirin.112.359

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