Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes-Reference-Cited by-同舟云学术

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Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes

Published:2015 Issue:4 Volume:20 Page:230
ISSN:2287-1012
Container-title:Annals of Pediatric Endocrinology & Metabolism
language:en
Short-container-title:Ann Pediatr Endocrinol Metab

Author:

Jeong Hyun Ah¹,Park Yoon Kyoung¹,Jung Yeong Sang¹,Nam Myung-Hyun²,Nam Hyo-Kyoung³,Lee Kee Hyoung³,Rhie Young-Jun¹

Affiliation:

1. Department of Pediatrics, Korea University Ansan Hospital, Korea University College of Medicine, Ansan, Korea.

2. Department of Laboratory Medicine, Korea University College of Medicine, Seoul, Korea.

3. Korea University College of Medicine, Seoul, Korea.

Publisher

Korean Society of Pediatric Endocrinology

Subject

Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Link

http://e-apem.org/upload/pdf/apem-20-230.pdf

Reference20 articles.

1. A Salt Wasting Syndrome in Infancy

2. Mineralocorticoid resistance

3. Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I

4. Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1

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1. Renal Tubular Acidosis in the Neonate;NeoReviews;2024-02-01

2. Clinical features, genetic background, and outcome in infants with urinary tract infection and type IV renal tubular acidosis;Pediatric Research;2019-12-18

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