Amelocerebrohypohidrotic syndrome

Kohlschütter-TC6nz syndrome (KTS) is a genetically heterogeneous autosomal recessive syndrome characterized by the triad of amelogenesis imperfect, infantile onset epilepsy, intellectual disability with or without regression and dementia.

Also known as: Kohlschutter-Tonz syndrome, amelocerebrohypohidrotic syndrome, epilepsy-dementia-amelogenesis imperfecta syndrome, KOHLSCHUTTER-Tonz syndrome, KTZS, Kohlschutter Tonz syndrome, Kohlschutter syndrome, epilepsy and Yellow teeth

0 clinical trials for this condition and its sub-types, 0 tagged with Amelocerebrohypohidrotic syndrome itself.