SUN-017 Impact of Steroid Precursors and Minor Metabolites Quantified by LC-MS-MS on Salt Wasting in 21-Hydroxylase Deficient Patients

Congenital adrenal hyperplasia (CAH), associated with 21-hydroxylase deficiency (21OHD), is a severe autosomic recessive disease. It may lead to life-threatening adrenal insufficiency with cortisol and aldosterone secretion defect, requiring hormone replacement therapy with hydrocortisone and fludro...

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Detalles Bibliográficos
Autores principales: Travers Allard, Simon, Bouvattier, Claire, Fagart, Jerome, Martinerie, Laetitia, Viengchareun, Say, Pussard, Eric, Lombes, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Steroid Hormones and Receptors
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6553069/
http://dx.doi.org/10.1210/js.2019-SUN-017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6553069/
http://dx.doi.org/10.1210/js.2019-SUN-017

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