Mitochondrial disorders and the eye

被引:39
|
作者
Kisilevsley, Eli [1 ]
Freund, Paul [1 ]
Margolin, Edward [1 ]
机构
[1] Univ Toronto, Dept Ophthalmol & Vis Sci, Toronto, ON, Canada
关键词
Eye; Kearns Sayre Syndrome; mitochondria; dominant optic atrophy; chronic progressive external ophthalmoplegia; MELAS; Leber hereditary optic neuropathy; HEREDITARY OPTIC NEUROPATHY; KEARNS-SAYRE-SYNDROME; PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; STROKE-LIKE EPISODES; RETINAL GANGLION-CELL; CEREBRAL FOLATE-DEFICIENCY; HUMAN EXTRAOCULAR-MUSCLES; LARGE BRAZILIAN PEDIGREE; FIBER LAYER EVALUATION; CHROMOSOME 3Q REGION;
D O I
10.1016/j.survophthal.2019.11.001
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Mitochondria are cellular organelles that play a key role in energy metabolism and oxidative phosphorylation. Malfunctioning of mitochondria has been implicated as the cause of many disorders with variable inheritance, heterogeneity of systems involved, and varied phenotype. Metabolically active tissues are more likely to be affected, causing an anatomic and physiologic disconnect in the treating physicians' mind between presentation and underlying pathophysiology. We shall focus on disorders of mitochondrial metabolism relevant to an ophthalmologist. These disorders can affect all parts of the visual pathway (crystalline lens, extraocular muscles, retina, optic nerve, and retrochiasm). After the introduction reviewing mitochondrial structure and function, each disorder is reviewed in detail, including approaches to its diagnosis and most current management guidelines. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:294 / 311
页数:18
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