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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...

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Detalles Bibliográficos
Autores principales:	Jeong, Hyun Ah, Park, Yoon Kyoung, Jung, Yeong Sang, Nam, Myung-Hyun, Nam, Hyo-Kyoung, Lee, Kee Hyoung, Rhie, Young-Jun
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Society of Pediatric Endocrinology 2015
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4722164/ https://www.ncbi.nlm.nih.gov/pubmed/26817011 http://dx.doi.org/10.6065/apem.2015.20.4.230

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