Arthrogryposis multiplex congenita associated with lissencephaly: a case report

Neuropediatrics. 1988 Feb;19(1):24-6. doi: 10.1055/s-2008-1052396.

Abstract

A child with arthrogryposis multiplex congenita and microcephaly is described. Cranial CT-scan and MRI showed abnormalities consistent with type I lissencephaly. The lissencephaly seems to be the primary cause of the congential contractures. Lissencephaly associated with arthrogryposis multiplex congenita has to be considered as a special kind of lissencephaly syndrome.

Publication types

  • Case Reports

MeSH terms

  • Arthrogryposis / complications*
  • Arthrogryposis / genetics
  • Arthrogryposis / physiopathology
  • Brain / abnormalities*
  • Brain / diagnostic imaging
  • Child, Preschool
  • Chromosome Deletion
  • Chromosomes, Human, Pair 21
  • Electromyography
  • Female
  • Humans
  • Tomography, X-Ray Computed