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Article

Prevalence of mild apparent mineralocorticoid excess in Mennonites.

The Journal of clinical endocrinology and metabolism - 1 Dec 1999

Ugrasbul F, Wiens T, Rubinstein P, New M I, Wilson R C

Abstract excerpt

UNLABELLED: We have studied an unusual patient with mild low-renin hypertension due to a homozygous mutation in the HSD11B2 gene (PNAS 95:10200-10205, 1998). The patient came from an inbred Mennonite family, and though the mutation identified her as an AME patient, she had a normal birth weight and did not demonstrate the typical features of AME, such as hypokalemic alkalosis, low birth weight, failure to thrive,...

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Identifiers

PMID: 10599743
DOI: 10.1210/jcem.84.12.6340

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

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