Gitelman Syndrome: A Rare Cause of Seizure Disorder and a Systematic Review
Author:
Affiliation:
1. Resident Physician, Louis Weiss Memorial Hospital, Chicago, IL, USA
2. Independent Research Scholar, Fauji Foundation Hospital, Rawalpindi, Pakistan
3. Resident Physician, Abington Hospital-Jefferson Health, Abington, PA, USA
Abstract
Publisher
Hindawi Limited
Subject
General Medicine
Link
http://downloads.hindawi.com/journals/crim/2019/4204907.pdf
Reference106 articles.
1. Persistent severe hypokalemia: Gitelman syndrome and differential diagnosis
2. Acquired Gitelman syndrome in a primary Sjögren syndrome patient with a SLC12A3 heterozygous mutation: A case report and literature review
3. Novel mutation in the SLC12A3 gene in a Sri Lankan family with Gitelman syndrome & coexistent diabetes: a case report
4. Acquired Gitelman Syndrome in an Anti-SSA Antibody-positive Patient with a SLC12A3 Heterozygous Mutation
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1. A case of Gitelman syndrome with homozygous SLC12A3 deletion presenting with epilepsy;Acta Epileptologica;2023-11-29
2. Novel Compound Heterozygous Mutations of the SLC12A3 Gene in Gitelman Syndrome with Growth Hormone Deficiency and Hypothyroidism;Iranian Journal of Pediatrics;2023-10-08
3. Tophaceous gout in a young man with Gitelman syndrome: a case report with an overview;Clinical Rheumatology;2022-09-27
4. NMDA Autoimmune Encephalitis and Severe Persistent Hypokalemia in a Pregnant Woman;Brain Sciences;2022-02-05
5. Gitelman syndrome: A first published clinical association with chronic pancreatitis, a case report and review of literature;International Journal of Surgery Case Reports;2022-02
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