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.

Kearns-Sayre Syndrome

Prevalence: 1/100000

mitochondrial

Official·OMIM:530000 Official·ORPHA480

PEO, retinal pigmentation, and cardiac conduction defect due to large-scale mtDNA deletions.

Associated Genes

No gene records found associated with this disease.