Rare Case of Adult‐Onset Gitelman Syndrome in a Patient With Multiple Comorbidities: A Case Report

ABSTRACT Gitelman Syndrome (GS) is a renal tubulopathy transmitted in an autosomal recessive manner. Its primary cause is mutations Of SLC12A3 (Solute Carrier Family 12 Member 3) gene that encodes the sodium‐chloride co‐transporter and is characterized by hypokalemia, hypocalciuria, hypomagnesemia,...

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Main Authors: Md. Deluwar Hussen, Fareha Rezwana, Merazul Islam Ony, Fariha Sultana, Fabeha Akter Joba, Zareen Tabassum
Format: Article
Language:English
Published: Wiley 2025-03-01
Series:Clinical Case Reports
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Online Access:https://doi.org/10.1002/ccr3.70323
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