Curation DMD DMD
0 + 0 = 0 / 18
Genetic evidence
Total: 0
Category | Type | Citation | Score | Details |
|---|---|---|---|---|
Singular Evidence | Probands | 0 | Single three-generation family reported with a DMD intron 62 GAA expansion (~59-82 repeats); two affected female relatives had chronic myopathy/dystrophinopathy-compatible findings, but the paper states that the repeat's phenotypic impact remains unresolved. | |
Collective Evidence | Computational | 0 | Large population analysis found proposed pathogenic genotypes at 4.705% in gnomAD males and 0.089% in gnomAD females, with similar expanded alleles in HPRC long-read data; these frequencies greatly exceed DMD prevalence, supporting the conclusion that the repeat expansion is unlikely to be pathogenic. |
Experimental evidence
Total: 0
No experimental evidence details available.
References
Direct supporting references for info on this page.