Evidence map›Paper›PMID 40162138›Full record

ArticleOxford medical case reports2025

Case report of atypical presentation of Bartter's syndrome: hypertension and Hypokalemic nephropathy in a female patient.

Emad A Odeh, Jaber H Jaradat, Raghad Amro, Seif Jankhout, Abdulqadir J Nashwan

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In one paragraph

Article in Oxford medical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Emad A OdehDepartment of Internal Medicine, Nephrology Department, Al-Basheer Hospital, Jordanian Ministry of health, Jabal al-Ashrafiyeh, At Taj Street, Amman Qasabah District, Amman 11151, Jordan.
Jaber H JaradatFaculty of Medicine, Mutah University, Karak Qasabah District, Mu'tah St, Al Karak 61710, Jordan.ORCID https://orcid.org/0000-0002-6488-4664
Raghad AmroFaculty of Medicine, Mutah University, Karak Qasabah District, Mu'tah St, Al Karak 61710, Jordan.ORCID https://orcid.org/0000-0002-1575-2550
Seif JankhoutFaculty of Medicine, Mutah University, Karak Qasabah District, Mu'tah St, Al Karak 61710, Jordan.ORCID https://orcid.org/0009-0004-9071-0512
Abdulqadir J NashwanNursing Department, Hamad Medical Corporation, Hamad Medical City, Al Rayyan Road, Doha 3050, Qatar.ORCID https://orcid.org/0000-0003-4845-4119

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bartter's syndrome (BS) is a rare hereditary disorder characterized by tubulopathies that affect salt reabsorption in the thick ascending limb of the Henle's loop. While BS typically presents with electrolyte imbalances and normal blood pressure, atypical presentations can complicate its diagnosis and management. We report the case of a 21-year-old female with BS diagnosed clinically at birth who presented with cough, vomiting, and elevated blood pressure. Despite a positive family history of BS, her presentation was unique with hypertension and hypokalemic nephropathy. Diagnostic evaluations during hospital admission revealed electrolyte imbalances, kidney dysfunction, and renal histopathological findings that were consistent with hypokalemic nephropathy. This case highlights the diverse clinical manifestations and potential complications of BS and emphasizes the importance of thorough evaluation and multidisciplinary management. Further research is needed to elucidate the underlying mechanisms linking BS with hypertension and hypokalemic nephropathy, and to guide targeted therapeutic strategies for complex presentations.

Indexed as

Bartter’s syndromecase reportelectrolyte imbalancehypertensionhypokalemic nephropathy

Identifiers

PMID40162138
PMCPMC11952896

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