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

Authors :
Christodoulou, J
Hall, R K
Menahem, S
Hopkins, I J
Rogers, J G
Source :
Journal of Medical Genetics; Dec1988, Vol. 25 Issue 12, p827-830, 4p, 2 Black and White Photographs, 1 Diagram, 1 Chart
Publication Year :
1988

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. [ABSTRACT FROM PUBLISHER]

Details

Language :
English
ISSN :
00222593
Volume :
25
Issue :
12
Database :
Complementary Index
Journal :
Journal of Medical Genetics
Publication Type :
Academic Journal
Accession number :
66011558