Neuro-Ophthalmic Manifestations of Pediatric Neurodegenerative Disease

被引:1
|
作者
Heidary, Gena [1 ]
机构
[1] Harvard Med Sch, Boston Childrens Hosp, Dept Ophthalmol, Boston, MA USA
关键词
HEREDITARY OPTIC NEUROPATHY; NEURONAL CEROID-LIPOFUSCINOSES; PELIZAEUS-MERZBACHER DISEASE; MITOCHONDRIAL-DNA MUTATION; COBALAMIN C DEFICIENCY; STROKE-LIKE EPISODES; ATAXIA-TELANGIECTASIA; OCULOMOTOR APRAXIA; METHYLMALONIC ACIDURIA; OCULAR MANIFESTATIONS;
D O I
10.1097/WNO.0000000000000549
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The topic of pediatric neurodegenerative disease is broad and ever expanding. Children who suffer from neurodegenerative disease often have concomitant visual dysfunction. Neuro-ophthalmologists may become involved in clinical care to identify corroborating eye findings when a specific condition is suspected, to monitor for disease progression, and in some cases, to assess treatment efficacy. Ophthalmic findings also may be the harbinger of a neurodegenerative process so a keen awareness of the possible manifestations of these conditions is important. The purpose of this review is to highlight common examples of the neuro-ophthalmic manifestations of pediatric neurodegenerative disease using a case-based approach in an effort to provide a framework for approaching these complex patients. (C) 2017 by North American Neuro-Ophthalmology Society
引用
收藏
页码:S4 / S13
页数:10
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