Living‐donor kidney transplantation for a patient with hypoparathyroidism, deafness, and renal dysplasia syndrome

Introduction Hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome is an autosomal dominant rare genetic disease. Some patients with hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome may present with renal calcification (nephrocalcinosis) and disorder. We re...

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Bibliographic Details

Published in:	IJU Case Reports
Main Authors:	Nobutaka Nishimura, Shunta Hori, Chihiro Omori, Makito Miyake, Satoshi Anai, Kazumasa Torimoto, Katsuya Aoki, Nobumichi Tanaka, Tatsuo Yoneda, Kiyohide Fujimoto
Format:	Article
Language:	English
Published:	Wiley 2020-11-01
Subjects:	GATA3 mutation HDR syndrome kidney transplantation nephrocalcinosis
Online Access:	https://doi.org/10.1002/iju5.12205