Mitochondrial dysfunction and neuromuscular disease

被引:3
作者
Nardin, RA [1 ]
Johns, DR [1 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Inst Med,Dept Neurol, Boston, MA 02115 USA
关键词
D O I
10.1002/1097-4598(200102)24:2<170::AID-MUS30>3.0.CO;2-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Mitochondrial diseases are a heterogeneous group of disorders with widely varying clinical features, due to defects in mitochondrial function. Involvement of both muscle and nerve is common in mitochondrial disease. In some cases, this involvement is subclinical or a minor part of a multisystem disorder. but myopathy and neuropathy are a major, often presenting, feature of a number of mitochondrial syndromes. In addition, mitochondrial dysfunction may play a role in a number of classic neuromuscular diseases. This article reviews the role of mitochondrial dysfunction in neuromuscular disease and discusses a rational approach to diagnosis and treatment of patients presenting with a neuromuscular syndrome due to mitochondrial disease. (C) 2001 John Wiley & Sons, Inc.
引用
收藏
页码:170 / 191
页数:22
相关论文
共 225 条
  • [1] Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA
    Andreu, AL
    Hanna, MG
    Reichmann, H
    Bruno, C
    Penn, AS
    Tanji, K
    Pallotti, F
    Iwata, S
    Bonilla, E
    Lach, B
    Morgan-Hughes, J
    DiMauro, S
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (14) : 1037 - 1044
  • [2] PHOSPHORUS MAGNETIC-RESONANCE SPECTROSCOPY (P-31 MRS) IN NEUROMUSCULAR DISORDERS
    ARGOV, Z
    BANK, WJ
    [J]. ANNALS OF NEUROLOGY, 1991, 30 (01) : 90 - 97
  • [3] TREATMENT OF MITOCHONDRIAL MYOPATHY DUE TO COMPLEX-III DEFICIENCY WITH VITAMINS K3 AND C - A P-31-NMR FOLLOW-UP-STUDY
    ARGOV, Z
    BANK, WJ
    MARIS, J
    ELEFF, S
    KENNAWAY, NG
    OLSON, RE
    CHANCE, B
    [J]. ANNALS OF NEUROLOGY, 1986, 19 (06) : 598 - 602
  • [4] DEPLETION OF MUSCLE MITOCHONDRIAL-DNA IN AIDS PATIENTS WITH ZIDOVUDINE-INDUCED MYOPATHY
    ARNAUDO, E
    DALAKAS, M
    SHANSKE, S
    MORAES, CT
    DIMAURO, S
    SCHON, EA
    [J]. LANCET, 1991, 337 (8740) : 508 - 510
  • [5] INVESTIGATION OF HUMAN MITOCHONDRIAL MYOPATHIES BY PHOSPHORUS MAGNETIC-RESONANCE SPECTROSCOPY
    ARNOLD, DL
    TAYLOR, DJ
    RADDA, GK
    [J]. ANNALS OF NEUROLOGY, 1985, 18 (02) : 189 - 196
  • [6] Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin
    Babcock, M
    deSilva, D
    Oaks, R
    DavisKaplan, S
    Jiralerspong, S
    Montermini, L
    Pandolfo, M
    Kaplan, J
    [J]. SCIENCE, 1997, 276 (5319) : 1709 - 1712
  • [7] MATERNALLY TRANSMITTED DIABETES AND DEAFNESS ASSOCIATED WITH A 10.4 KB MITOCHONDRIAL-DNA DELETION
    BALLINGER, SW
    SHOFFNER, JM
    HEDAYA, EV
    TROUNCE, I
    POLAK, MA
    KOONTZ, DA
    WALLACE, DC
    [J]. NATURE GENETICS, 1992, 1 (01) : 11 - 15
  • [8] MYOINTESTINAL, NEUROINTESTINAL, GASTROINTESTINAL ENCEPHALOPATHY (MNGIE SYNDROME) DUE TO PARTIAL DEFICIENCY OF CYTOCHROME-C-OXIDASE - A NEW MITOCHONDRIAL MULTISYSTEM DISORDER
    BARDOSI, A
    CREUTZFELDT, W
    DIMAURO, S
    FELGENHAUER, K
    FRIEDE, RL
    GOEBEL, HH
    KOHLSCHUTTER, A
    MAYER, G
    RAHLF, G
    SERVIDEI, S
    VANLESSEN, G
    WETTERLING, T
    [J]. ACTA NEUROPATHOLOGICA, 1987, 74 (03) : 248 - 258
  • [9] RECURRENT RESPIRATORY INSUFFICIENCY AND DEPRESSED VENTILATORY DRIVE COMPLICATING MITOCHONDRIAL MYOPATHIES
    BAROHN, RJ
    CLANTON, T
    SAHENK, Z
    MENDELL, JR
    [J]. NEUROLOGY, 1990, 40 (01) : 103 - 106
  • [10] Barrientos A, 1996, AM J HUM GENET, V58, P963