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Article

Non-functioning adrenal incidentalomas caused by 21-hydroxylase deficiency or carrier status?

Endocrine - 1 Sept 2014

Falhammar Henrik

Abstract excerpt

Adrenal incidentalomas (AI) are an escalating clinical issue due to the increasing use of imaging techniques. Occasional patients with AIs have been reported who have subsequently been diagnosed with congenital adrenal hyperplasia (CAH) due to CYP21A2 mutations (21-hydroxylase deficiency) or carr...

Topics

Adrenal Gland Neoplasms
Adrenal Hyperplasia, Congenital
Adult
Aged
Aged, 80 and over
Female
Genetic Predisposition to Disease
Heterozygote
Humans
Male
Middle Aged
Middle East
Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Retrospective Studies

Steroid 21-Hydroxylase

Sweden

Source

Identifiers

PMID: 24452876
DOI: 10.1007/s12020-013-0162-1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-24452876-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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