Progressive External Ophthalmoplegia

被引:54
|
作者
McClelland, Collin [1 ,2 ]
Manousakis, Georgios [3 ]
Lee, Michael S. [1 ,2 ,3 ,4 ]
机构
[1] Univ Minnesota, Dept Ophthalmol, 420 Delaware St SE MMC 493, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Visual Neurosci, 420 Delaware St SE MMC 493, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Neurol, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Dept Neurosurg, Minneapolis, MN 55455 USA
关键词
Mitochondrial myopathy; Progressive external ophthalmoplegia; KEARNS-SAYRE-SYNDROME; MITOCHONDRIAL-DNA DELETIONS; SENSORINEURAL HEARING-LOSS; IMPAIR MTDNA REPLICATION; EXTRAOCULAR-MUSCLES; OPTIC ATROPHY; CLINICAL-FEATURES; OPA1; MUTATIONS; DIAGNOSIS; DISEASE;
D O I
10.1007/s11910-016-0652-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Progressive external ophthalmoplegia (PEO), marked by progressive bilateral ptosis and diffuse reduction in ocular motility, represents a finding of mitochondrial myopathy rather than a true diagnosis. PEO often occurs with other systemic features of mitochondrial dysfunction that can cause significant morbidity and mortality. Accurate and early recognition of PEO is paramount for the optimal care of these patients. We present an evidence-based review of the presenting neuroophthalmic features, differential diagnosis, diagnostic tools, systemic implications, and treatment options for isolated PEO and other PEO-associated mitochondrial syndromes.
引用
收藏
页数:10
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