CellWell record HH-50442
Clinical and genetic features in 30 children with Gitelman syndrome
Qian-Qian Sheng; Shu-Min He; Gui-Xia Ding
2026
In plain language
In 30 Chinese children with genetically confirmed Gitelman syndrome, all had hypokalemia and 90 percent had low magnesium, with fatigue and short stature the most common clinical features.
- Evidence
- Emerging
- Design
- Primary research (design unspecified)
Cite this record: https://thecellwell.org/studies/HH-50442
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