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Article

Bartter syndrome and growth hormone deficiency: three cases.

Pediatric nephrology (Berlin, Germany) - 1 Nov 2012

Buyukcelik Mithat, Keskin Mehmet, Kilic Beltinge Demircioglu, Kor Yilmaz, Balat Ayse

Abstract excerpt

BACKGROUND: Bartter syndrome is a rare autosomal recessive disorder characterized by hypokalemia, salt loss, and metabolic alkalosis. Short stature is one of the clinical manifestations in these children. Although polyuria, polydipsia, hypokalemia, and salt loss may be responsible for growth retardation, the exact pathogenesis of short stature in Bartter syndrome is not known. CASE DIAGNOSIS AND TREATMENT: In...

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PMID: 22707176
DOI: 10.1007/s00467-012-2212-y

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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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