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A Rare Case of Pseudohypoaldosteronism Type II or Gordon Syndrome

Introduction: Pseudohypoaldosteronism type II (PHA II) or Gordon Syndrome is a rare, autosomally inherited disease with unknown prevalence. It is caused by mutations in the WNK1, WNK4, CUL3, or KLHL3 gene. It is characterized by hypertension, hyperkalemia, hyperchloremic metabolic acidosis and low p...

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Detalles Bibliográficos
Autores principales:	Manas, F N U, Mandal, Shobha, Mols-Kowalczewski, Barbara L
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2021
Materias:	Adrenal
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8089166/ http://dx.doi.org/10.1210/jendso/bvab048.210

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