The information on this page is for informational purposes only and does not constitute medical advice. Consult your genetic counselor or specialist physician for treatment decisions.

Oculopharyngeal Muscular Dystrophy

Prevalence: 1/100000
neuromuscular
Official·OMIM:164300Official·ORPHA270

Eyelid drooping and swallowing difficulty due to PABPN1 gene mutations.

Associated Genes

No gene records found associated with this disease.