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1.
Neurology ; 37(7): 1209-11, 1987 Jul.
Article in English | MEDLINE | ID: mdl-3601084

ABSTRACT

Development of epilepsy was studied prospectively in a group of 77 consecutive stroke patients. Included were stroke patients less than 75 years old admitted within the first 3 days after the stroke. Excluded were patients with subarachnoid hemorrhage, vertebrobasilar stroke, and patients with other severe diseases. Cerebral angiography, CT, and EEG were performed in all patients. The patients were followed clinically for 2 to 4 years. Seven patients (9%) developed epilepsy. Of 23 patients with lesions involving the cortex, 6 (26%) developed epilepsy. Of 54 patients in whom the cortex was not involved, only 1 (2%) developed epilepsy. Patients with persisting paresis and cortical involvement seem to be at particularly high risk of developing epilepsy, as 50% of such patients (6 of 12) developed the disease.


Subject(s)
Brain/diagnostic imaging , Cerebrovascular Disorders/complications , Epilepsy/etiology , Adult , Aged , Cerebral Angiography , Cerebrovascular Disorders/diagnostic imaging , Electroencephalography , Epilepsy/diagnostic imaging , Female , Humans , Male , Middle Aged , Prospective Studies , Risk , Tomography, X-Ray Computed
3.
J Neurol Sci ; 64(2): 137-48, 1984 May.
Article in English | MEDLINE | ID: mdl-6747661

ABSTRACT

A family with the clinical features of Behr's syndrome is described that exhibited probable pseudodominant inheritance. The salient clinical manifestations consisted of mental retardation and dementia, optic atrophy, cerebellar ataxia, pyramidal signs and peripheral neuropathy. Nerve biopsy from the index case showed a chronic neuropathy with axonal degeneration and regeneration. A muscle biopsy from the same patient demonstrated multiple inclusions composed of spiral cylindrical structures possibly derived from the sarcoplasmic reticulum, and less obtrusive accumulations of mitochondria, some of which contained paracrystalline inclusions.


Subject(s)
Cerebellar Diseases/genetics , Intellectual Disability/genetics , Nerve Degeneration , Spinal Cord Diseases/genetics , Vision Disorders/genetics , Adolescent , Adult , Biopsy , Cerebellar Diseases/pathology , Child , Consanguinity , Female , Humans , Infant, Newborn , Intellectual Disability/pathology , Male , Middle Aged , Muscles/pathology , Spinal Cord Diseases/pathology , Sural Nerve/pathology , Syndrome , Vision Disorders/pathology
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