Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Aplasia cutis congenita
Aplasia cutis-myopia syndrome
Aplasia cutis-myopia syndrome is characterized by the association of aplasia cutis congenita with high myopia, congenital nystagmus and cone-rod dysfunction. It has been described in two siblings (brother and sister). Transmission is autosomal dominant.
This condition has no sub-types.