Genotypic spectrum of 21-hydroxylase deficiency in an endogamous population.
Rana Abdelhakim Ahmed MahmoudN H AmrN N ToaimaT M KamalH H ElsedfyPublished in: Journal of endocrinological investigation (2021)
Molecular characterization should be considered along with clinical and biochemical diagnosis of CAH since it could confirm the diagnosis, outline the treatment strategy and morbidity, and ensure proper genetic counseling.