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Kearns-Sayre syndrome

MONDO:0010787

Kearns-Sayre syndrome (KSS) is a mitochondrial disease characterized by progressive external ophthalmoplegia (PEO), pigmentary retinitis and an onset before the age of 20 years. Common additional features include deafness, cerebellar ataxia and heart block.

Also known as: Kearns Sayre Syndrome, Kearns-Sayre syndrome, CPEO with myopathy, CPEO with ragged red fibers, CPEO with ragged red fibres, CPEO with ragged-Red fibers, CPEO with ragged-Red fibres, KSS

34 clinical trials for this condition and its sub-types, 5 tagged with Kearns-Sayre syndrome itself.

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