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

@article{Christodoulou1988ASO,
  title={A syndrome of epilepsy, dementia, and amelogenesis imperfecta: genetic and clinical features.},
  author={John Christodoulou and Roger K. Hall and Samuel Menahem and Ian Hopkins and John G. Rogers},
  journal={Journal of medical genetics},
  year={1988},
  volume={25 12},
  pages={827-30}
}
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. 

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