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 r...

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Vydáno v:IJU Case Rep
Hlavní autoři: Nishimura, Nobutaka, Hori, Shunta, Omori, Chihiro, Miyake, Makito, Anai, Satoshi, Torimoto, Kazumasa, Aoki, Katsuya, Tanaka, Nobumichi, Yoneda, Tatsuo, Fujimoto, Kiyohide
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2020
Témata:
Case Reports
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7609182/
https://ncbi.nlm.nih.gov/pubmed/33163915
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/iju5.12205
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