Article

Managing Gitelman Syndrome: Socioeconomic Barriers and Clinical Outcomes

2024-12-10

Abstract excerpt

Gitelman syndrome (GS) is a rare autosomal recessive renal tubulopathy characterized by hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria due to mutations in the SLC12A3 gene. This case report presents a 54-year-old African American female with near syncope and palpitations. The patient had a history of intermittent palpitations and generalized anxiety disorder and was previously diagnosed with GS...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: ed87ff32-f0b0-5bc9-beaa-62ab2a132efa
DOI: 10.20944/preprints202412.0813.v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Managing Gitelman Syndrome: Socioeconomic Barriers and Clinical OutcomesDOI 10.20944/preprints202412.0813.v1Read

Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.Semantic proximity Read

[Expert consensus for the diagnosis and treatment of patients with Gitelman syndrome].Semantic proximity Read

Gitelman Syndrome in a Pregnant WomanSemantic proximity Read

The Electrolyte Enigma: Unmasking Gitelman Syndrome in a Patient With Recurrent Hypokalemic Paralysis Episodes, A Case ReportSemantic proximity Read

Gitelman syndrome: pathophysiological and clinical aspects.Semantic proximity Read

Gitelman syndrome.Semantic proximity Read

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

Novel SLC12A3 mutation in Gitelman syndrome.Semantic proximity Read

Gitelman syndrome with primary hyperparathyroidism: A case report.Semantic proximity Read

Clinical phenotypic and genotypic analysis of Gitelman syndrome in childrenSemantic proximity Read

Gitelman's syndrome: a pathophysiological and clinical update.Semantic proximity Read

Novel heterozygous mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome: A care-compliant case report.Semantic proximity Read