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🔗 CustomizeMedical Overview of Gitelman-Like Kidney Tubulopathy Due To Mitochondrial DNA Mutation
Sources citedA rare genetic renal tubular disease characterized by hypomagnesemia (due to renal magnesium wasting), hypokalemia and activation of renin production due to specific mitochondrial DNA mutations. Hypocalciuria, metabolic alkalosis, progressive chronic kidney disease as well as arterial hypertension and hypercholesterolemia have been reported. Tetany, tremor, paresthesia, muscle fatigue, chondrocalcinosis and cerebral seizures can be present. Extrarenal manifestations of mitochondrial dysfuntion may not be evident in the patients.
Classification & codes: GARD 0022486 · Orphanet ORPHA:620371 · ICD-10 N15.8
Sources: GARD (NIH/NCATS), Orphanet · last reviewed 2026. Educational only — not medical advice.
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Care & management overview — Gitelman-Like Kidney Tubulopathy Due To Mitochondrial DNA Mutation
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Gitelman-Like Kidney Tubulopathy Due To Mitochondrial DNA Mutation News & Developments
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Companies Developing Treatments
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Certified Centers of Excellence
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Sources: GARD (NIH/NCATS), Orphanet · last reviewed 2026. Educational only — not medical advice.