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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Detalles Bibliográficos
Autores principales: Nishimura, Nobutaka, Hori, Shunta, Omori, Chihiro, Miyake, Makito, Anai, Satoshi, Torimoto, Kazumasa, Aoki, Katsuya, Tanaka, Nobumichi, Yoneda, Tatsuo, Fujimoto, Kiyohide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7609182/
https://www.ncbi.nlm.nih.gov/pubmed/33163915
http://dx.doi.org/10.1002/iju5.12205

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7609182/
https://www.ncbi.nlm.nih.gov/pubmed/33163915
http://dx.doi.org/10.1002/iju5.12205

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