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

Anand Sheya

Anand Sheya

Department of Endocrinology and Metabolism, Sri Ramachandra Institute of Higher Education and ResearchChennai, India
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Sheya, Anand
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Nayana Tara Vasireddy

Nayana Tara Vasireddy

Department of Endocrinology and Metabolism, Sri Ramachandra Institute of Higher Education and ResearchChennai, India
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Vasireddy, Nayana Tara
, 
Shriraam Mahadevan

Shriraam Mahadevan

Department of Endocrinology and Metabolism, Sri Ramachandra Institute of Higher Education and ResearchChennai, India
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Mahadevan, Shriraam
, 
Asha Ranjan

Asha Ranjan

Department of Endocrinology and Metabolism, Sri Ramachandra Institute of Higher Education and ResearchChennai, India
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Ranjan, Asha
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Adlyne Reena Asirvatham

Adlyne Reena Asirvatham

Department of Endocrinology and Metabolism, Sri Ramachandra Institute of Higher Education and ResearchChennai, India
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Asirvatham, Adlyne Reena
 y 
Sai Namratha Gogineni

Sai Namratha Gogineni

Department of Endocrinology and Metabolism, Sri Ramachandra Institute of Higher Education and ResearchChennai, India
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Gogineni, Sai Namratha
  
28 ago 2025
Phenotypic spectrum and diagnostic challenges in non-21-alpha-hydroxylase deficiency congenital adrenal hyperplasia: a case series from a tertiary care center's Cover Image
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Publicado en línea: 28 ago 2025
Páginas: 135 - 140
DOI: https://doi.org/10.2478/enr-2025-0015
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© 2025 Anand Sheya et al., published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
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1 veces al año
Temas de la revista:
Ciencias de la vida, Biología molecular, Neurobiología, Medicina, Ciencias médicas básicas, Ciencias médicas básicas, otros, Medicina Clínica, Medicina Interna, Endocrinología, diabetología
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