Challenges in Diagnosing Rhabdomyolysis: Lesson Learned from a Patient with a Mitochondrial DNA Mutation (P7-11.001)
To describe the clinical, neuropathological, and genetic features of a patient with recurrent rhabdomyolysis due to a variant in mitochondrial DNA (mtDNA)
Authors
- Emanuele Barca (ORCID: https://orcid.org/0009-0007-6672-6524)
- Nuri Jacoby (ORCID: https://orcid.org/0000-0001-9152-8860)
- Kurenai Tanji (ORCID: https://orcid.org/0000-0003-2230-2416)
- Michael Miller (ORCID: https://orcid.org/0000-0003-0781-7868)
- Ali Naini (ORCID: https://orcid.org/0000-0002-8030-1115)
- Michio Hirano (ORCID: https://orcid.org/0000-0002-7070-7402)
- Saba Tadesse
Institutions
- Maimonides Medical Center (US)
- Columbia University Irving Medical Center (US)
Publication Details
- Journal
- Neurology
- Published
- 2025-04-07
- DOI
- https://doi.org/10.1212/wnl.0000000000211133
- Primary Topic
- Muscle and Compartmental Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00