A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysis

被引:44
作者
Chinnery, PF
Johnson, MA
Taylor, RW
Lightowlers, RN
Turnbull, DM
机构
[1] UNIV NEWCASTLE UPON TYNE,SCH MED,DEPT NEUROL,NEWCASTLE TYNE NE2 4HH,TYNE & WEAR,ENGLAND
[2] UNIV NEWCASTLE UPON TYNE,DEPT NEUROBIOL,NEWCASTLE TYNE NE2 4HH,TYNE & WEAR,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1002/ana.410410319
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We describe a patient who presented with acute rhabdomyolysis and had 68% cytochrome c oxidase (COX)-deficient fibers in skeletal muscle. Further investigations confirmed a respiratory chain defect that was associated with a novel heteroplasmic point mutation in the phenylalanine tRNA gene of the mitochondrial genome (mtDNA). Analysis of single muscle fibers revealed a significantly greater level of mutant mtDNA in COX-negative fibers. This is the first case of a mitochondrial tRNA gene point mutation presenting with acute rhabdomyolysis and recurrent myoglobinuria.
引用
收藏
页码:408 / 410
页数:3
相关论文
共 15 条
  • [1] SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME
    ANDERSON, S
    BANKIER, AT
    BARRELL, BG
    DEBRUIJN, MHL
    COULSON, AR
    DROUIN, J
    EPERON, IC
    NIERLICH, DP
    ROE, BA
    SANGER, F
    SCHREIER, PH
    SMITH, AJH
    STADEN, R
    YOUNG, IG
    [J]. NATURE, 1981, 290 (5806) : 457 - 465
  • [2] MUSCLE CARNITINE PALMITYLTRANSFERASE DEFICIENCY AND MYOGLOBINURIA
    DIMAURO, S
    DIMAURO, PMM
    [J]. SCIENCE, 1973, 182 (4115) : 929 - 931
  • [3] ACUTE PERIPHERAL NEUROPATHY, RHABDOMYOLYSIS, AND SEVERE LACTIC-ACIDOSIS ASSOCIATED WITH 3243 A TO G MITOCHONDRIAL-DNA MUTATION
    HARA, H
    WAKAYAMA, Y
    KOUNO, Y
    YAMADA, H
    TANAKA, M
    OZAWA, T
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1994, 57 (12) : 1545 - 1546
  • [4] CYTOCHROME-C-OXIDASE ACTIVITY IN SINGLE MUSCLE-FIBERS - ASSAY TECHNIQUES AND DIAGNOSTIC APPLICATIONS
    JOHNSON, MA
    BINDOFF, LA
    TURNBULL, DM
    [J]. ANNALS OF NEUROLOGY, 1993, 33 (01) : 28 - 35
  • [5] A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria
    Keightley, JA
    Hoffbuhr, KC
    Burton, MD
    Salas, VM
    Johnston, WSW
    Penn, AMW
    Buist, NRM
    Kennaway, NG
    [J]. NATURE GENETICS, 1996, 12 (04) : 410 - 416
  • [6] MORAES CT, 1993, J CLIN INVEST, V92, P2906, DOI 10.1172/JCI116913
  • [7] MUSCLE COENZYME-Q DEFICIENCY IN FAMILIAL MITOCHONDRIAL ENCEPHALOMYOPATHY
    OGASAHARA, S
    ENGEL, AG
    FRENS, D
    MACK, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (07) : 2379 - 2382
  • [8] VERY LONG-CHAIN ACYL COENZYME-A DEHYDROGENASE-DEFICIENCY PRESENTING WITH EXERCISE-INDUCED MYOGLOBINURIA
    OGILVIE, I
    POURFARZAM, M
    JACKSON, S
    STOCKDALE, C
    BARTLETT, K
    TURNBULL, DM
    [J]. NEUROLOGY, 1994, 44 (03) : 467 - 473
  • [9] MITOCHONDRIAL-DNA DELETIONS IN INHERITED RECURRENT MYOGLOBINURIA
    OHNO, K
    TANAKA, M
    SAHASHI, K
    IBI, T
    SATO, W
    YAMAMOTO, T
    TAKAHASHI, A
    OZAWA, T
    [J]. ANNALS OF NEUROLOGY, 1991, 29 (04) : 364 - 369
  • [10] PENN AS, 1994, MYOLOGY