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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 adolescent girl presenting with episodes of carpopedal spasms and difficulty in walking with laboratory tests suggestive of...

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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 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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