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Kearns–Sayre syndrome
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Genetic mitochondrial disease
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Kearns–Sayre syndrome (KSS), oculocraniosomatic disorder or oculocranionsomatic neuromuscular disorder with ragged red fibers is a mitochondrial myopathy with a typical onset before 20 years of age. KSS is a more severe syndromic variant of chronic progressive external ophthalmoplegia (abbreviated CPEO), a syndrome that is characterized by...

Instance of
head and neck disease
developmental defect during embryogenesis
class of disease
Signs and symptoms
Subclass of
neurometabolic disease
syndromic genetic deafness
Wikidata