Antenatal Diagnosis and Treatment in Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency and Congenital Adrenal Hyperplasia Screening in Newborns

Signs of virilization, such as clitoromegaly, labio-scrotal fusion, and urogenital sinus may be observed in females with 21-hydroxylase deficiency (21-OHD) and other rare virilizing forms of congenital adrenal hyperplasia (CAH). This makes sex determination difficult, and multiple reconstructive sur...

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Bibliografiset tiedot

Päätekijät:	Zehra Yavaş Abalı, Erdal Kurnaz, Tülay Güran
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	Pediatric Endocrinology and Diabetes Society 2025-01-01
Sarja:	JCRPE
Aiheet:	congenital adrenal hyperplasia 21-hydroxylase deficiency antenatal diagnosis antenatal dexamethasone newborn screening
Linkit:	https://jag.journalagent.com/z4/download_fulltext.asp?pdir=jcrpe&un=JCRPE-58661
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