A familial syndrome of unilateral polymicrogyria affecting the right hemisphere

Neurology. 2006 Jan 10;66(1):133-5. doi: 10.1212/01.wnl.0000191393.06679.e9.

Abstract

A number of familial syndromes of bilateral polymicrogyria (PMG) have been described, but reported unilateral PMG cases have generally been sporadic. The authors identified four families in which unilateral right-sided PMG on MRI was present in more than one individual, with pathologic confirmation in one. Core clinical features included contralateral hemiparesis, developmental delay, and focal seizures. The authors' findings suggest that unilateral PMG exists in a familial syndrome of probable germline genetic origin.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Cerebral Cortex / abnormalities*
  • Child
  • Child, Preschool
  • Developmental Disabilities / diagnosis
  • Developmental Disabilities / genetics
  • Developmental Disabilities / physiopathology
  • Epilepsies, Partial / diagnosis
  • Epilepsies, Partial / genetics
  • Family Health
  • Female
  • Functional Laterality / genetics*
  • Genetic Predisposition to Disease / genetics*
  • Humans
  • Inheritance Patterns / genetics
  • Intellectual Disability / diagnosis
  • Intellectual Disability / genetics
  • Intellectual Disability / physiopathology
  • Magnetic Resonance Imaging
  • Male
  • Nervous System Malformations / diagnosis*
  • Nervous System Malformations / genetics*
  • Neurofibromatosis 1 / complications
  • Neurofibromatosis 1 / genetics
  • Paresis / diagnosis
  • Paresis / genetics
  • Paresis / physiopathology
  • Pedigree
  • Syndrome