Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria

BACKGROUND: 3β-hydroxysteroid dehydrogenase 2 (3βHSD2) deficiency is a rare form of congenital adrenal hyperplasia (CAH), with fewer than 200 cases reported in the world literature and few data on outcomes. PATIENTS AND METHODS: We report a mixed longitudinal and cross-sectional study from a single...

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Detalles Bibliográficos
Autores principales: Ladjouze, Asmahane, Donaldson, Malcolm, Plotton, Ingrid, Djenane, Nacima, Mohammedi, Kahina, Tardy-Guidollet, Véronique, Mallet, Delphine, Boulesnane, Kamélia, Bouzerar, Zair, Morel, Yves, Roucher-Boulez, Florence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229600/
https://www.ncbi.nlm.nih.gov/pubmed/35757411
http://dx.doi.org/10.3389/fendo.2022.867073

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229600/
https://www.ncbi.nlm.nih.gov/pubmed/35757411
http://dx.doi.org/10.3389/fendo.2022.867073

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