Clinical and Hormonal Profile of Classical 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia: Experience from a Tertiary Centre In India

Clinical and Hormonal Profile of Classical 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia: Experience from a Tertiary Centre In India

Introduction: Congenital adrenal hyperplasia (CAH) is a rare autosomal recessive disorder requiring treatment with steroids. Both over and under-treatment can have an impact on growth outcomes. Aims: The aim of this study was to study the clinical and hormonal profile of a cohort of individua...

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Bibliographic Details
Main Authors: Harshitha Boyareddy, Pramila Kalra, Mala Dharmalingam
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-08-01
Series:Indian Journal of Endocrinology and Metabolism
Subjects:
17-oh progesterone; 21-alpha-hydroxylase; ambiguous genitalia; congenital adrenal hyperplasia (cah); growth outcomes; height; salt wasting
Online Access:https://journals.lww.com/indjem/fulltext/2024/07000/clinical_and_hormonal_profile_of_classical.12.aspx

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https://journals.lww.com/indjem/fulltext/2024/07000/clinical_and_hormonal_profile_of_classical.12.aspx

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