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Article

A rare case of Gitelman's syndrome with hypophosphatemia.

Journal of the College of Physicians and Surgeons--Pakistan : JCPSP - 1 Apr 2009

Akhtar Naureen, Hafeez Farkhanda

Abstract excerpt

Gitelman's syndrome is a hereditary disorder occurring due to loss of functional mutations of the gene encoding the distal convoluted tubule sodium chloride cotransporter (NCCT) and is characterized by hypokalemic metabolic alkalosis, hypomagnesemia and hypocalciuria. This case reports an adolesc...

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Identifiers

PMID: 19356345
DOI: 04.2009/JCPSP.257259

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19356345-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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