Limb-girdle muscular dystrophy D3: The first North American family and review of the literature
Limb-girdle muscular dystrophy type D3 is a rare, late-onset muscular dystrophy that has, to date, only been identified in European, South American, and Asian populations. Here we present the index patient of the first North American family with LGMDD3. We review this disorder and highlight both common and uncommon clinical features. We also discuss new insights into disease pathogenesis.
Authors
- Adam S. Deardorff (ORCID: https://orcid.org/0000-0002-0042-0991)
- Michael C Isfort
Institutions
- Wright State University (US)
- The Ohio State University Wexner Medical Center (US)
Publication Details
- Journal
- Journal of the Neurological Sciences
- Published
- 2025-08-22
- DOI
- https://doi.org/10.1016/j.jns.2025.123670
- Primary Topic
- Muscle Physiology and Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00