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Hemimegalencephaly: diagnosis and treatment.

Abstract
Three boys with hemimegalencephaly are reported. Two suffered neonatal convulsions and the third presented with seizures at seven months. In each case the EEG was grossly abnormal, with spike and wave activity. All three have significant developmental delay and demonstrate other manifestations of the condition: macrocephaly in two, contralateral hemiparesis in one and one boy has ipsilateral facial hemihypertrophy and linear naevus. Hemimegalencephaly can be recognised on cranial ultrasonography, and the seizures may respond to benzodiazepine therapy.
AuthorsJ Q Trounce, N Rutter, D H Mellor
JournalDevelopmental medicine and child neurology (Dev Med Child Neurol) Vol. 33 Issue 3 Pg. 261-6 (Mar 1991) ISSN: 0012-1622 [Print] England
PMID1902803 (Publication Type: Case Reports, Journal Article)
Topics
  • Adolescent
  • Adult
  • Cerebral Cortex (abnormalities)
  • Child
  • Child, Preschool
  • Dominance, Cerebral (physiology)
  • Epilepsies, Partial (diagnostic imaging)
  • Facial Hemiatrophy (diagnostic imaging)
  • Follow-Up Studies
  • Humans
  • Male
  • Neurologic Examination
  • Radiography

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