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Renal insufficiency caused by TMEM216 gene mutation: Case Report
Lingjun Sun1, Meiqi Xu1, Xiaoying Deng2
1Department of Nephrology, The Second Hospital of Dalian Medical University, Dalian, Liaoning, China.
Frontiers in Medicine
|May 14, 2025
Summary
Genetic mutations in the TMEM216 gene are linked to severe chronic kidney disease (CKD) progression. Early genetic testing is crucial for diagnosing unexplained CKD in young patients and enabling personalized treatment strategies.
Area of Science:
- Nephrology
- Genetics
- Ciliopathies
Background:
- Chronic kidney disease (CKD) is a global health issue with high morbidity, often progressing to end-stage renal disease (ESRD).
- Genetic factors are increasingly recognized in unexplained renal dysfunction, with mutations in ciliopathy-related genes like TMEM216 implicated in severe kidney impairment.
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