Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
A rare inherited muscular dystrophy characterized by the coexistence of limb-girdle weakness and early-onset diffuse joint contractures without cardiomyopathy.
No clinical trials have been registered for Emery-Dreifuss-like muscular dystrophy.
4 publications have been identified in PubMed for Emery-Dreifuss-like muscular dystrophy. Research spans Case Report / Case Series (50%), Epidemiology / Natural History (25%), and Gene Therapy / Novel Therapeutics (25%).
Elkoush A (2026). [PMID: 42047848](https://pubmed.ncbi.nlm.nih.gov/42047848/). *J Neurol*. [Epidemiology / Natural History]
Cattin E (2025). [PMID: 40940734](https://pubmed.ncbi.nlm.nih.gov/40940734/). *Cells*. [Gene Therapy / Novel Therapeutics]
Valoriani F (2024). [PMID: 38742022](https://pubmed.ncbi.nlm.nih.gov/38742022/). *Frontiers in nutrition*. [Case Report / Case Series]
Debnath A (2024). [PMID: 39737306](https://pubmed.ncbi.nlm.nih.gov/39737306/). *Cureus*. [Case Report / Case Series]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 6:04 PM UTC
Common questions about Emery-Dreifuss-like muscular dystrophy