A classification scheme for malformations of cortical development

被引:345
作者
Barkovich, AJ
Kuzniecky, RI
Dobyns, WB
Jackson, GD
Becker, LE
Evrard, P
机构
[1] UNIV ALABAMA,DEPT NEUROL,EPILEPSY CTR,BIRMINGHAM,AL 35294
[2] UNIV MINNESOTA,MED CTR,DEPT CHILD NEUROL,MINNEAPOLIS,MN 55455
[3] UNIV LONDON,INST CHILD HLTH,LONDON WC1N 1EH,ENGLAND
[4] HOSP SICK CHILDREN,DEPT PATHOL,TORONTO,ON M5G 1X8,CANADA
[5] UNIV CATHOLIQUE LOUVAIN,CLIN UNIV ST LUC,PEDIAT NEUROL SERV,B-1200 BRUSSELS,BELGIUM
关键词
agyria; heterotopia; Lissencephaly; neuronal migration; polymicrogyria;
D O I
10.1055/s-2007-973750
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Malformations of the cerebral cortex are being recognized more frequently as a cause of epilepsy, developmental delay, neurological deficits, and mental retardation. Nonetheless, a standard nomenclature and classification system of these malformations, based upon state-of the art knowledge derived from genetics, embryology, imaging, and pathology, has not been devised. In this manuscript, we propose such a classification system. Moreover, we have constructed the system such that both the framework and the classifications themselves are flexible and can be adapted as our knowledge of the embryology! genetics, imaging, and pathology of these disorders advances. We believe that the use of this classification system will help both clinicians and researchers to understand and think about these disorders and their causes better. In turn, we hope that this improved understanding will lead to further refinements in classification, to advances in our knowledge and, ultimately, to improvements in therapy.
引用
收藏
页码:59 / 63
页数:5
相关论文
共 53 条
  • [21] CAUSAL HETEROGENEITY IN ISOLATED LISSENCEPHALY
    DOBYNS, WB
    ELIAS, ER
    NEWLIN, AC
    PAGON, RA
    LEDBETTER, DH
    [J]. NEUROLOGY, 1992, 42 (07) : 1375 - 1388
  • [22] LISSENCEPHALY AND OTHER MALFORMATIONS OF CORTICAL DEVELOPMENT - 1995 UPDATE
    DOBYNS, WB
    TRUWIT, CL
    [J]. NEUROPEDIATRICS, 1995, 26 (03) : 132 - 147
  • [23] LISSENCEPHALY - A HUMAN BRAIN MALFORMATION ASSOCIATED WITH DELETION OF THE LIS1 GENE LOCATED AT CHROMOSOME-17P13
    DOBYNS, WB
    REINER, O
    CARROZZO, R
    LEDBETTER, DH
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 270 (23): : 2838 - 2842
  • [24] THE NEUROGENETICS OF LISSENCEPHALY
    DOBYNS, WB
    [J]. NEUROLOGIC CLINICS, 1989, 7 (01) : 89 - 105
  • [25] DOBYNS WB, 1995, IN PRESS BRAIN DEV
  • [26] MECHANISM OF ARREST OF NEURONAL MIGRATION IN ZELLWEGER MALFORMATION - HYPOTHESIS BASED UPON CYTOARCHITECTONIC ANALYSIS
    EVRARD, P
    CAVINESS, VS
    PRATSVINAS, J
    LYON, G
    [J]. ACTA NEUROPATHOLOGICA, 1978, 41 (02) : 109 - 117
  • [27] Evrard P, 1989, CHILD NEUROLOGY DEV, P153
  • [28] NEUROPATHOLOGIC FINDINGS IN CORTICAL RESECTIONS (INCLUDING HEMISPHERECTOMIES) PERFORMED FOR THE TREATMENT OF INTRACTABLE CHILDHOOD EPILEPSY
    FARRELL, MA
    DEROSA, MJ
    CURRAN, JG
    SECOR, DL
    CORNFORD, ME
    COMAIR, YG
    PEACOCK, WJ
    SHIELDS, WD
    VINTERS, HV
    [J]. ACTA NEUROPATHOLOGICA, 1992, 83 (03) : 246 - 259
  • [29] THE GLIAL FASCICLE - AN ONTOGENIC AND PHYLOGENIC UNIT GUIDING, SUPPLYING AND DISTRIBUTING MAMMALIAN CORTICAL-NEURONS
    GRESSENS, P
    EVRARD, P
    [J]. DEVELOPMENTAL BRAIN RESEARCH, 1993, 76 (02): : 272 - 277
  • [30] GUERRINI R, 1992, DEV MED CHILD NEUROL, V34, P706