Clinical and molecular characteristics of simple virilizing congenital adrenal hyperplasia due to 21-hydroxylase deficiency: insight from a tertiary pediatric center in Vietnam

Purpose Simple virilizing congenital adrenal hyperplasia (SV-CAH) due to 21-hydroxylase deficiency (21-OHD) is an autosomal recessive disease caused by pathogenic variants of the CYP21A2 gene. Children with SV-CAH often experience delayed diagnosis, presenting with pseudo-precocious puberty in males...

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Autors principals:	Khanh Ngoc Nguyen, Giang Thi Kim Dang, Ngoc Thi Bich Can, Dien Minh Tran, Thao Phuong Bui, Mai Nguyen Thi Phuong, Huong Thu Pham, Ngoc Diem Ngo, Dung Chi Vu
Format:	Artigo
Idioma:	Inglês
Publicat:	Korean Society of Pediatric Endocrinology 2025-12-01
Col·lecció:	Annals of Pediatric Endocrinology & Metabolism
Matèries:	simple virilizing congenital adrenal hyperplasia 21-hydroxylase deficiency
Accés en línia:	http://e-apem.org/upload/pdf/apem-2448292-146.pdf
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