Phenotypic spectrum and diagnostic challenges in non-21-alpha-hydroxylase deficiency congenital adrenal hyperplasia: a case series from a tertiary care center Cover

Phenotypic spectrum and diagnostic challenges in non-21-alpha-hydroxylase deficiency congenital adrenal hyperplasia: a case series from a tertiary care center

Endocrine Regulations

Volume 59 (2025): Issue 1 (January 2025)

By:

Anand Sheya, Nayana Tara Vasireddy, Shriraam Mahadevan, Asha Ranjan, Adlyne Reena Asirvatham and Sai Namratha Gogineni

Open Access

|Aug 2025

Download Article

Download the full article as a PDF file.

DOI: https://doi.org/10.2478/enr-2025-0015 | Journal eISSN: 1336-0329 | Journal ISSN: 1210-0668

Journal RSS Feed

Language: English

Page range: 135 - 140

Published on: Aug 28, 2025

Published by: Slovak Academy of Sciences

In partnership with: Paradigm Publishing Services

Publication frequency: 1 times per year

Keywords:

non-21-OHD CAH,

congenital adrenal hyperplasia,

genetic disorders,

young hypertension

Related subjects:

Molecular biology,

Basic medical science,

Basic medical science, other,

Clinical medicine,

Internal medicine,

Endocrinology, diabetology

© 2025 Anand Sheya, Nayana Tara Vasireddy, Shriraam Mahadevan, Asha Ranjan, Adlyne Reena Asirvatham, Sai Namratha Gogineni, published by Slovak Academy of Sciences
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Previous article Volume 59 (2025): Issue 1 (January 2025)Next article