COMPLEX-I (REDUCED NICOTINAMIDE-ADENINE DINUCLEOTIDE COENZYME-Q REDUCTASE) DEFICIENCY IN 2 PATIENTS WITH PROBABLE LEIGH SYNDROME

被引:46
作者
FUJII, T
ITO, M
OKUNO, T
MUTOH, K
NISHIKOMORI, R
MIKAWA, H
机构
[1] Department of Pediatrics, Kyoto University, Faculty of Medicine, Kyoto
关键词
D O I
10.1016/S0022-3476(05)81650-6
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Two infants who had clinical and radiographic findings consistent with Leigh syndrome were found to have deficiency of complex I (reduced nicotinamideadenine dinucleotide-coenzyme Q reductase) activity. Significant abnormalities were found on computed tomographic scans and magnetic resonance images of the brain. Lactate and pyruvate concentrations in blood and cerebrospinal fluid were elevated, and muscle biopsy specimens showed abnormal mitochondria. These data indicate that Leigh syndrome, as well as MELAS syndrome (mitochondrial encephalopathy, myopathy, lactic acidosis, and stroke-like episodes) may result from complex I deficiency. © 1990 The C. V. Mosby Company.
引用
收藏
页码:84 / 87
页数:4
相关论文
共 18 条
  • [1] MEASUREMENT OF CYTOCHROMES IN HUMAN SKELETAL-MUSCLE MITOCHONDRIA, ISOLATED FROM FRESH AND FROZEN STORED MUSCLE SPECIMENS
    BOOKELMAN, H
    TRIJBELS, JMF
    SENGERS, RCA
    JANSSEN, AJM
    [J]. BIOCHEMICAL MEDICINE, 1978, 19 (03): : 366 - 373
  • [2] NECROTIZING ENCEPHALOMYELOPATHY OF LEIGH - NEUROPATHOLOGICAL FINDINGS IN 8 CASES
    DAYAN, AD
    OCKENDEN, BG
    CROME, L
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1970, 45 (239) : 39 - &
  • [3] CYTOCHROME-C-OXIDASE DEFICIENCY IN LEIGH SYNDROME
    DIMAURO, S
    SERVIDEI, S
    ZEVIANI, M
    DIROCCO, M
    DEVIVO, DC
    DIDONATO, S
    UZIEL, G
    BERRY, K
    HOGANSON, G
    JOHNSEN, SD
    JOHNSON, PC
    [J]. ANNALS OF NEUROLOGY, 1987, 22 (04) : 498 - 506
  • [4] FARMER TW, 1973, NEUROLOGY, V23, P429
  • [5] LEIGHS ENCEPHALOMYELOPATHY - AN INBORN ERROR OF GLUCONEOGENESIS
    HOMMES, FA
    POLMAN, HA
    REERINK, JD
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1968, 43 (230) : 423 - &
  • [6] FINDINGS IN MUSCLE IN COMPLEX-I (NADH COENZYME-Q REDUCTASE) DEFICIENCY
    KOGA, Y
    NONAKA, I
    KOBAYASHI, M
    TOJYO, M
    NIHEI, K
    [J]. ANNALS OF NEUROLOGY, 1988, 24 (06) : 749 - 756
  • [7] KRETZSCHMAR HA, 1987, PEDIATRICS, V79, P370
  • [9] DEFECT IN SUCCINATE OXIDATION BY ISOLATED MUSCLE MITOCHONDRIA IN A PATIENT WITH SYMMETRICAL LESIONS IN THE BASAL GANGLIA
    MARTIN, JJ
    VANDEVYVER, FL
    SCHOLTE, HR
    ROODHOOFT, AM
    CEUTERICK, C
    MARTIN, L
    LUYTHOUWEN, IEM
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1988, 84 (2-3) : 189 - 200
  • [10] SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY - REVIEW AND A STUDY OF 2 FAMILIES
    MONTPETIT, VJ
    ANDERMANN, F
    CARPENTER, S
    FAWCETT, JS
    ZBOROWSK.D
    GIBERSON, HR
    [J]. BRAIN, 1971, 94 : 1 - +