Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation-Reference-Cited by-同舟云学术

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Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation

Published:2019-03-27 Issue:4 Volume:24 Page:489-490
ISSN:1320-5358
Container-title:Nephrology
language:en
Short-container-title:Nephrology

Author:

Tanaka Tatsuhiko¹,Oki Eishin²,Mori Takayasu³,Tsuruga Kazushi¹,Sohara Eisei³,Uchida Shinichi³,Tanaka Hiroshi¹⁴

Affiliation:

1. Department of PediatricsHirosaki University Hospital Aomori Japan

2. Department of PediatricsTsugaru General Hospital Aomori Japan

3. Department of Nephrology, Graduate School of Medical and Dental SciencesTokyo Medical and Dental University Tokyo Japan

4. Department of School Health ScienceHirosaki University Faculty of Education Aomori Japan

Publisher

Wiley

Subject

Nephrology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nep.13391

Reference4 articles.

1. Clinical features and molecular basis of pseudohypoaldosteronism type 1

2. Autosomal Dominant Pseudohypoaldosteronism Type 1: Mechanisms, Evidence for Neonatal Lethality, and Phenotypic Expression in Adults

3. Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1

4. Clinical and molecular analysis of six Japanese patients with a renal form of pseudohypoaldosteronism type 1

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1. Rare forms of genetic paediatric adrenal insufficiency: Excluding congenital adrenal hyperplasia;Reviews in Endocrine and Metabolic Disorders;2023-02-10

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