A rare case report about a congenital adrenal hyperplasia by 21-hydroxylase lock in its pure virilizing form discovered in adolescence

INTRODUCTION: Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is an autosomal recessive disease. The diagnosis of the classic virilizing form must be made at birth. CASE PRESENTATION: We report the case of a 16-year-old female patient, who consulted for primary amenorrhea and a...

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Detalles Bibliográficos
Autores principales: Alla, Achwak, Draoui, Najat, Rami, Imane, Rouf, Siham, Saadi, Hanane, Kamaoui, Imane, Latrech, Hanane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9111920/
https://www.ncbi.nlm.nih.gov/pubmed/35592826
http://dx.doi.org/10.1016/j.amsu.2022.103673

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9111920/
https://www.ncbi.nlm.nih.gov/pubmed/35592826
http://dx.doi.org/10.1016/j.amsu.2022.103673

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