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Demyelinating radiculopathy in the kearns-sayre syndrome: A clinicopathological study

โœ Scribed by Dennis R. Groothuis; Sidney Schulman; Robert Wollman; James Frey; Nicholas A. Vick


Publisher
John Wiley and Sons
Year
1980
Tongue
English
Weight
876 KB
Volume
8
Category
Article
ISSN
0364-5134

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High proportions of mtDNA duplications i
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Kearns-Sayre syndrome (KSS) is a sporadic multisystem mitochondrial disorder characterized by progressive external ophthalmoplegia, pigmentary retinopathy, onset before age 20, and severe cardiac conduction defects that can lead to death. KSS patients harbor partial deletions of mitochondrial DNA (โŒฌ