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Article

[Premature androgenetic alopecia in adult male with nonclassic 21-OH deficiency. A novel nonsense CYP21A2 mutation (Y336X) in 2 affected siblings].

Medicina clinica - 28 Oct 2006

Bernal González Carmen, Fernández Salas Carmen, Martínez Silvia, Ezquieta Zubicaray Begoña

Abstract excerpt

BACKGROUND AND OBJECTIVE: Nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency mainly manifests with symptoms and signs of hyperandrogenism, which are usually obvious in women and sometimes obvious in children or adolescents, but are rarely observed in adult men especially with increasing age. Male pattern alopecia is considered an androgenetic and age-related symptom. However, its early...

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Identifiers

PMID: 17145028
DOI: 10.1016/s0025-7753(06)72688-4

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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[Premature androgenetic alopecia in adult male with nonclassic 21-OH deficiency. A novel nonsense CYP21A2 mutation (Y336X) in 2 affected siblings].PMID 17145028Read ↗

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[Analysis of CYP21A2 gene mutations in two families with 21-hydroxylase deficiency].Semantic proximity Read ↗

[Health status of adults with congenital adrenal hyperplasia due to 21-hydroxylase deficiency].Semantic proximity Read ↗

[Analysis of CYP21A2 gene mutation in one case of congenital adrenal hyperplasia].Semantic proximity Read ↗

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