A rare case report about a congenital adrenal hyperplasia by 21-hydroxylase lock in its pure virilizing form discovered in adolescence.
Ann Med Surg (Lond)
; 78: 103673, 2022 Jun.
Article
en En
| MEDLINE
| ID: mdl-35592826
17OHP, 17 hydroxyprogesterone; 21-Hydroxylase deficiency; ACTH, Adrenocorticotropic Hormone; CAH, Congenital adrenal hyperplasia; CMIA, Chemiluminescence microparticle immunology; CPA, Cyproterone Acetate; CYP21, the gene encoding 21-hydroxylase, a cytochrome P-450 enzyme; Case report; Congenital adrenal hyperplasia; PCR, Polymerase Chain Reaction; Pure virilizing form; SDHEA, Dehydroepiandrosterone Sulfate
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Idioma:
En
Revista:
Ann Med Surg (Lond)
Año:
2022
Tipo del documento:
Article
País de afiliación:
Marruecos
Pais de publicación:
Reino Unido