Epilepsy and anomalies of neuronal migration: MRI and clinical aspects

Neuronal migration disorders are the result of disturbed brain development. In such disorders, neurons are abnormally located. In diagnosing these conditions, magnetic resonance imaging is superior to any other imaging technique. This enables us to improve our knowledge of the clinical correlates of neuronal migration. With reference to migrational disorder, a retrospective study of all 303 patients with epileptic seizures referred for magnetic resonance imaging during a 3‐year period was performed, 13 patients (aged 12–41, mean age 27) were identified. They represent 4.3 % of the entire study group. Of the patients with known epilepsy, 6.7% and of the mentally retarded, 13.7% had migrational disorders. Four patients had schizencephaly as the dominant finding, one was classified as hemimegalencephaly, 2 had isolated heterotopias, and 6 had localized pachy‐and/or poly‐microgyria. The clinical pictures are complex. Ectopias of grey matter are recognised foci of epilepsy, but from an epileptological and a clinical viewpoint little attention has been given to these disorders. The present study shows that malmigration is not rare in epilepsy patients, especially not in the mentally retarded.

[1]  D. Norman,et al.  MR imaging of schizencephaly. , 1988, AJR. American journal of roentgenology.

[2]  R. Kuzniecky,et al.  Focal cortical myoclonus and rolandic cortical dysplasia: Clarification by magnetic resonance imaging , 1988, Annals of neurology.

[3]  F Andermann,et al.  Generalized cortical dysplasia manifested by diffusely thick cerebral cortex. , 1989, Archives of Neurology.

[4]  M. Mikhael,et al.  Malformation of the cerebral cortex with heterotopia of the gray matter. , 1978, Journal of computer assisted tomography.

[5]  W. Dobyns,et al.  Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly. , 1984, American journal of medical genetics.

[6]  D. Janz,et al.  Neuropathological Findings in Primary Generalized Epilepsy: A Study of Eight Cases , 1984, Epilepsia.

[7]  J. Manson,et al.  Fukuyama Congenital Muscular Dystrophy In Two Australian Female Siblings , 1990, Developmental medicine and child neurology.

[8]  H Gastaut,et al.  Considerations on the Significance Attributed to Unusual Cerebral Histological Findings Recently Described in Eight Patients with Primary Generalized Epilepsy , 1985, Epilepsia.

[9]  S. Chuang,et al.  Unilateral megalencephaly: correlation of MR imaging and pathologic characteristics. , 1990, AJNR. American journal of neuroradiology.

[10]  R. Kuzniecky,et al.  Bilateral central macrogyria: Epilepsy, pseudobulbar palsy, and mental retardation—a recognizable neuronal migration disorder , 1989, Annals of neurology.

[11]  B. Harding,et al.  Unknown syndrome: pachygyria, joint contractures, and facial abnormalities. , 1989, Journal of medical genetics.

[12]  P. Rakic,et al.  Neuronal migration and contact guidance in the primate telencephalon. , 1978, Postgraduate medical journal.

[13]  W. Arts,et al.  Diagnostic Features And Clinical Signs Of 21 Patients With Lissencephaly Type I , 1990, Developmental medicine and child neurology.

[14]  R. Quencer,et al.  Association of heterotopic gray matter with seizures: MR imaging. Work in progress. , 1988, Radiology.

[15]  J. Opitz,et al.  Syndromes with lissencephaly. II: Walker-Warburg and cerebro-oculo-muscular syndromes and a new syndrome with type II lissencephaly. , 1985, American journal of medical genetics.

[16]  J. Stears,et al.  Schizencephaly , 1984, Neurology.

[17]  J. Moore,et al.  Magnetic resonance imaging and neurobehavioral correlates in schizencephaly. , 1990, Archives of neurology.

[18]  D. Janz,et al.  The Significance of Microdysgenesia in Primary Generalized Epilepsy: An Answer to the Considerations of Lyon and Gastaut , 1985, Epilepsia.

[19]  D. Norman,et al.  MR of neuronal migration anomalies. , 1987, AJR. American journal of roentgenology.

[20]  A. Barkovich,et al.  Band heterotopias: a newly recognized neuronal migration anomaly. , 1989, Radiology.

[21]  J. Aicardi,et al.  Unusual M4RI appearance of diffuse subcortical heterotopia or "double cortex" in two children , 2022 .

[22]  M A Falconer,et al.  Focal dysplasia of the cerebral cortex in epilepsy , 1971, Journal of neurology, neurosurgery, and psychiatry.

[23]  S. Larson,et al.  MR imaging and positron emission tomography of cortical heterotopia. , 1985, Journal of computer assisted tomography.