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

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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Bibliographic Details
Main Authors: Zehra Yavaş Abalı, Erdal Kurnaz, Tülay Güran
Format: Article
Language:English
Published: Galenos Yayincilik 2025-01-01
Series:JCRPE
Subjects:
congenital adrenal hyperplasia
21-hydroxylase deficiency
antenatal diagnosis
antenatal dexamethasone
newborn screening
Online Access:https://jag.journalagent.com/z4/download_fulltext.asp?pdir=jcrpe&un=JCRPE-58661

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https://jag.journalagent.com/z4/download_fulltext.asp?pdir=jcrpe&un=JCRPE-58661

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