A syndrome of epilepsy, dementia, and amelogenesis imperfecta: genetic and clinical features

J Med Genet. 1988 Dec;25(12):827-30. doi: 10.1136/jmg.25.12.827.

Abstract

A family is described with six members affected by a syndrome of epilepsy, dementia, and amelogenesis imperfecta (Kohlschütter's syndrome). An autosomal recessive pattern of inheritance is established for this disorder.

Publication types

  • Case Reports

MeSH terms

  • Amelogenesis Imperfecta / genetics*
  • Amelogenesis Imperfecta / pathology
  • Child
  • Dementia / genetics*
  • Epilepsy / genetics*
  • Female
  • Genes, Recessive
  • Humans
  • Infant
  • Male
  • Pedigree
  • Syndrome