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Updated: May 29, 2025

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
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Adult-Onset Episodic Rhabdomyolysis in a Patient With a Heterozygous Lipin 1 (LPIN1) Mutation: A Case Report
Naman Bareja1, Rafail A Chionatos1, Camelia Valhuerdi Porto1
1Neurology, Tufts Medical Center, Boston, USA.
Cureus
|February 3, 2025
Summary
This study reports a rare case of adult-onset myopathy and rhabdomyolysis in a heterozygous Lipin-1 (LPIN1) carrier. It highlights the importance of considering LPIN1 mutations in adults with unexplained muscle symptoms.
Area of Science:
- Genetics
- Metabolic Disorders
- Neuromuscular Diseases
Background:
- Lipin-1 (LPIN1) is crucial for lipid metabolism.
- Mutations in LPIN1 typically cause pediatric rhabdomyolysis.
- Adult-onset presentations are rare but possible.
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