Neutral Lipid Storage Disease With Myopathy and Infiltrative Cardiomyopathy Initially Presenting as Right Arm Weakness
Neutral lipid storage disease with myopathy is a rare genetic syndrome of abnormal intracellular lipolysis leading to lipid droplet accumulation in skeletal and cardiac muscle. Because of variability in clinical presentations, a multidisciplinary approach is essential for diagnosis and treatment.
Authors
- Manjula Ananthram (ORCID: https://orcid.org/0009-0006-6361-6031)
- Rydhwana Hossain (ORCID: https://orcid.org/0000-0003-0907-3938)
- Diljon Chahal (ORCID: https://orcid.org/0000-0003-2717-1486)
- R. Michael Benitez
- Christopher C. Krogh
- Cinthia B. Drachenberg (ORCID: https://orcid.org/0000-0002-3104-5661)
- Justin Brilliant (ORCID: https://orcid.org/0000-0001-8946-268X)
- Anuj Gupta (ORCID: https://orcid.org/0000-0002-4252-5206)
- Brian Barr (ORCID: https://orcid.org/0000-0002-4424-3448)
- Neil Porter
Institutions
- University of Maryland, Baltimore (US)
Publication Details
- Journal
- JACC Case Reports
- Published
- 2024-12-01
- DOI
- https://doi.org/10.1016/j.jaccas.2024.102809
- Citations
- 3
- Primary Topic
- Lipid metabolism and biosynthesis
- Type
- article
- Field-Weighted Citation Impact
- 0.88