Article

Congenital Adrenal Hyperplasia Case Attending With Hypertension Diagnosed With 21OH Deficiency

2026-07-30

Abstract excerpt

<title>Abstract</title> <p> Background Congenital adrenal hyperplasia (CAH) is a group of disorders with autosomal recessive inheritance, characterized by diverse pathological gene variations in enzymes regulating steroid synthesis in the adrenal glands. Deficiency of 21-hydroxylase (21OHD) comprises nearly 95% of all CAH cases. This is followed by 11- <italic>β</italic> -hydroxylase deficiency (11OHD). In th...

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Literature Corpus work: b215bbdb-875f-5d7c-b78b-8ae31f657ffd
DOI: 10.21203/rs.3.rs-9961710/v1

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Congenital Adrenal Hyperplasia Case Attending With Hypertension Diagnosed With 21OH DeficiencyDOI 10.21203/rs.3.rs-9961710/v1Read

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