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Article

Hypertension in a patient with Gitelman's syndrome.

Journal of human hypertension - 1 Sept 2004

Ogihara T, Katsuya T, Ishikawa K, Matsuo A, Rakugi H, Shoji M, Yasujima M

Abstract excerpt

Gitelman's syndrome is an autosomal recessive disorder characterized by sodium wasting and hypotension. A middle-aged woman was diagnosed with Gitelman's syndrome because of typical clinical manifestations in the youth and homozygous mutations of 18-base-pair insertion in exon 6 of thiazide-sensi...

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Source

Identifiers

PMID: 15002004
DOI: 10.1038/sj.jhh.1001699

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15002004-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hypertension in a patient with Gitelman's syndrome.PMID 15002004Read ↗

Unexpected clinical sequelae of Gitelman syndrome: hypertension in adulthood is common and females have higher potassium requirements.Semantic proximity Read ↗

Gitelman Syndrome in a Pregnant WomanSemantic proximity Read ↗

Gitelman syndrome: pathophysiological and clinical aspects.Semantic proximity Read ↗

Case-control study of the role of the Gitelman's syndrome gene in essential hypertension.Semantic proximity Read ↗

Persistent hypokalemia due to a rare mutation in gitelman's syndrome.Semantic proximity Read ↗

Hypokalemic rhabdomyolysis in a child with Gitelman's syndrome.Semantic proximity Read ↗

A high prevalence of Gitelman's syndrome mutations in Japanese.Semantic proximity Read ↗

Inheritance of an autosomal recessive disorder, Gitelman's syndrome, across two generations in one family.Semantic proximity Read ↗

Thiazide-sensitive Na+-Cl- cotransporter: genetic polymorphisms and human diseases.Semantic proximity Read ↗

Resistance to Insulin in Patients with Gitelman Syndrome and a Subtle Intermediate Phenotype in Heterozygous Carriers: A Cross-Sectional StudySemantic proximity Read ↗

G2736A polymorphism of thiazide-sensitive Na-Cl cotransporter gene predisposes to hypertension in young women.Semantic proximity Read ↗

Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure.Semantic proximity Read ↗

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