Hypokalemic rhabdomyolysis in a child with Gitelman's syndrome. [electronic resource]
Producer: 20100618Description: 953-5 p. digitalISSN:- 1432-198X
- Adolescent
- Biomarkers -- blood
- Creatine Kinase -- blood
- DNA Mutational Analysis
- Female
- Fluid Therapy
- Gitelman Syndrome -- complications
- Humans
- Hypokalemia -- genetics
- Magnesium -- blood
- Mutation
- Potassium -- blood
- Receptors, Drug -- genetics
- Rhabdomyolysis -- genetics
- Solute Carrier Family 12, Member 3
- Symporters -- genetics
- Treatment Outcome
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Publication Type: Case Reports; Journal Article
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