A syndrome of epilepsy, dementia, and amelogenesis imperfecta: genetic and clinical features.
Open Access
- 1 December 1988
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 25 (12) , 827-830
- https://doi.org/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.This publication has 4 references indexed in Scilit:
- An in-vitro study of enamel protein degradation in developing bovine enamelArchives of Oral Biology, 1986
- Analysis of a kindred with amelogenesis imperfectaJournal of Oral Pathology & Medicine, 1985
- Hereditary amelogenesis imperfecta. I. Epidemiology and clinical classification in a Swedish child population.1985
- Familial epilepsy and yellow teeth--a disease of the CNS associated with enamel hypoplasia.1974