MON-268 A Rare Case of Primary Hypoaldosteronism in a Newborn

BACKGROUND: Primary aldosterone synthase deficiency (ASD) is a rare but potentially life-threatening cause of mineralocorticoid deficiency primarily due to a defect in CYP11B2, which encodes aldosterone synthase. There are two types of ASDs, both resulting in primary hypoaldosteronism, but due to di...

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Detalles Bibliográficos
Autores principales: Mody, Armaiti, Lee, Janet, Tenney, Jessica, Srinivasan, Shylaja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Pediatric Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550606/
http://dx.doi.org/10.1210/js.2019-MON-268

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550606/
http://dx.doi.org/10.1210/js.2019-MON-268

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