Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria
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DOI: 10.3389/fendo.2022.867073
Abstract: 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… read more here.
Keywords: hsd2; hydroxysteroid dehydrogenase; deficiency; deficiency algeria ... See more keywords