Phenotypic spectrum and diagnostic challenges in non-21-alpha-hydroxylase deficiency congenital adrenal hyperplasia: a case series from a tertiary care center
By:
Authors
Anand Sheya
Department of Endocrinology and Metabolism, Sri Ramachandra Institute of Higher Education and Research, Chennai, India
Nayana Tara Vasireddy
Department of Endocrinology and Metabolism, Sri Ramachandra Institute of Higher Education and Research, Chennai, India
Shriraam Mahadevan
Department of Endocrinology and Metabolism, Sri Ramachandra Institute of Higher Education and Research, Chennai, India
Asha Ranjan
Department of Endocrinology and Metabolism, Sri Ramachandra Institute of Higher Education and Research, Chennai, India
Adlyne Reena Asirvatham
Department of Endocrinology and Metabolism, Sri Ramachandra Institute of Higher Education and Research, Chennai, India
Sai Namratha Gogineni
Department of Endocrinology and Metabolism, Sri Ramachandra Institute of Higher Education and Research, Chennai, India
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
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© 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.