THE NEUROLOGIC MANIFESTATIONS OF MITOCHONDRIAL DISEASE

被引:16
作者
Parikh, Sumit [1 ]
机构
[1] Cleveland Clin, Cleveland, OH 44195 USA
关键词
mitochondria; mitochondrial disease; neurological; neuropathy; white matter; stroke; hearing loss; pigmentary retinopathy; Leigh syndrome; ataxia; Alper syndrome; POLG; epilepsia partialis continua-epilepsy; seizures; cerebellar degeneration; optic atrophy; myopathy; hypotonia; dysmotility; RIBOSOMAL-RNA MUTATION; DNA POLYMERASE-GAMMA; OXIDATIVE-PHOSPHORYLATION; OXIDASE DEFICIENCY; STATUS EPILEPTICUS; POLG MUTATIONS; LEIGH-SYNDROME; L-ARGININE; CHILDREN; DEPLETION;
D O I
10.1002/ddrr.110
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The nervous system contains some of the body's most metabolically demanding cells that are highly dependent on ATP produced via mitochondrial oxidative phosphorylation. Thus, the neurological system is consistently involved in patients with mitochondrial disease. Symptoms differ depending on the part of the nervous system affected. Although almost any neurological symptom can be due to mitochondrial disease, there are select symptoms that are more suggestive of a mitochondrial problem. Certain symptoms that have become sine qua non with underlying mitochondrial cytopathies can serve as diagnostic "red-flags." Here, the typical and atypical presentations of mitochondrial disease in the nervous system are reviewed, focusing on "red flag" neurological symptoms as well as associated symptoms that can occur in, but are not specific to, mitochondrial disease. The multitudes of mitochondria! syndromes are not reviewed in-depth, though a select few are discussed in some detail. (C) 2010 Wiley-Liss, Inc. Dev Disabil Res Rev 2010;16:120-128.
引用
收藏
页码:120 / 128
页数:9
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