Article
Epileptic encephalopathy and amelogenesis imperfecta: Kohlschütter-Tönz syndrome.
European journal of medical genetics - 1 May 2012
Schossig Anna, Wolf Nicole I, Kapferer Ines, Kohlschütter Alfried, Zschocke Johannes
Abstract excerpt
Kohlschütter-Tönz syndrome is a rare genetic disorder with epilepsy, psychomotor regression, and a severe enamel defect with yellow or brownish discoloration of the teeth. The first affected family was described in 1974, and 25 patients in 11 families have been reported until now. Inheritance is autosomal recessive. Epilepsy usually starts within the first or second year of life. All affected individuals show a...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
