Therapeutic needs from early childhood in four patients with 21-hydroxylase deficiency harboring the P30L mutation on one allele.

Itonaga, Tomoyo; Akiba, Kazuhisa; Hasegawa, Yukihiro

Itonaga, Tomoyo; Akiba, Kazuhisa; Hasegawa, Yukihiro.

Afiliación

Itonaga T; Division of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center (TMCMC), Tokyo, Japan.
Akiba K; Department of Pediatrics, Oita University Faculty of Medicine, Oita, Japan.
Hasegawa Y; Division of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center (TMCMC), Tokyo, Japan.

Clin Pediatr Endocrinol ; 30(4): 187-193, 2021.

Article en En | MEDLINE | ID: mdl-34629741

Palabras clave

21-hydroxylase deficiency; P30L; congenital adrenal hyperplasia; genotype-phenotype correlation; non-classical phenotype

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Clin Pediatr Endocrinol Año: 2021 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Japón

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