A case of atypical cholesterol side chain defect possibly caused by CYP11A1 heterozygous mutation / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
;
(12): 161-164, 2019.
Artículo
en Chino
| WPRIM
| ID: wpr-745704
ABSTRACT
This paper reports a case of atypical cholesterol side chain enzyme deficiency caused possibly by CYP11A1p.A359V heterozygous mutation. The patient was diagnosed as congenital adrenal hyperplasia because he was born with gonadal dysplasia and there were manifestations of salt losing and pigment changing, combined with high level of plasma ACTH. Further genetic screening revealed CYP11A1p.A359V heterozygous mutations in patients with a final diagnosis of cholesterol side chain enzyme deficiency which was treated effectively to glucocorticoid.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Idioma:
Chino
Revista:
Chinese Journal of Endocrinology and Metabolism
Año:
2019
Tipo del documento:
Artículo
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