The prevalence and genotype of 21-hydroxylase deficiency in the Croatian Romani population

OBJECTIVE: Congenital adrenal hyperplasia (CAH) owing to 21-hydroxylase deficiency (21-OHD) is a rare autosomal recessive disorder caused by pathological variants in the CYP21A2 gene. After a high prevalence of classic 21-OHD CAH in the Romani population was reported in the Republic of North Macedon...

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Detalles Bibliográficos
Autores principales: Dumic, Katja K., Grubic, Zorana, Kusec, Vesna, Braovac, Duje, Gotovac, Kristina, Vinkovic, Maja, Vucinic, Maja, Dumic, Miroslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266231/
https://www.ncbi.nlm.nih.gov/pubmed/37324261
http://dx.doi.org/10.3389/fendo.2023.1170449

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266231/
https://www.ncbi.nlm.nih.gov/pubmed/37324261
http://dx.doi.org/10.3389/fendo.2023.1170449

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