| Literature DB >> 2111767 |
Abstract
The autopsy of a 19-month-old boy with severe myoclonic epilepsy of infancy (SMEI) and sudden unexpected death (SUD) revealed several developmental brain abnormalities. The most striking features were microdysgenesis of cerebellum and cerebral cortex and threefold spinal cord channels with surrounding ectopic tissue. Hippocampus and brainstem were normal.Entities:
Mesh:
Year: 1990 PMID: 2111767 DOI: 10.1111/j.1528-1157.1990.tb05378.x
Source DB: PubMed Journal: Epilepsia ISSN: 0013-9580 Impact factor: 5.864