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

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

Hyponatremia and hyperkalemia in infancy can be attributed to various causes, originating from a variety of renal and genetic disorders. Pseudohypoaldosteronism type 1 (PHA1) is one of these disorders, causing mineralocorticoid resistance that results in urinary salt wasting, failure to thrive, meta...

Full description

Bibliographic Details
Main Authors: Hyun Ah Jeong, Yoon Kyoung Park, Yeong Sang Jung, Myung-Hyun Nam, Hyo-Kyoung Nam, Kee Hyoung Lee, Young-Jun Rhie
Format: Article
Language:English
Published: Korean Society of Pediatric Endocrinology 2015-12-01
Series:Annals of Pediatric Endocrinology & Metabolism
Subjects:
Pseudohypoaldosteronism
NR3C2 gene
Mineralocorticoid receptors
Hyponatremia
Hyperkalemia
Online Access:http://e-apem.org/upload/pdf/apem-20-230.pdf

Similar Items

Similar Items