Catalog
Kearns-Sayre syndrome
No MMS code
Link to WHO Definition
Kearns-Sayre syndrome – http://id.who.int/icd/entity/399100745
Kearns-Sayre syndrome is a mitochondrial neuromuscular disease characterised by an onset before the age of 20 years, ophthalmoplegia, ptosis and pigmentary retinitis.
Parents
- Certain specified primary disorders of muscles
- Large-scale single deletions of mitochondrial DNA
- 9C82.0 Progressive external ophthalmoplegia
- Syndrome with hypoparathyroidism
- LD2H Syndromic genetic deafness
- Syndromic conditions with disorders of intellectual development as a relevant clinical feature
- Syndromic corneal dystrophy