Mesh term Aicardi Syndrome
Browse to parent terms:Agenesis of Corpus Callosum
Congenital Abnormalities
Eye Diseases, Hereditary
Genetic Diseases, X-Linked
Description
A rare genetic disorder characterized by partial or complete absence of the CORPUS CALLOSUM, resulting in infantile spasms, MENTAL RETARDATION, and lesions of the RETINA or OPTIC NERVE.Search for this term in our Faculty Database
View this term at the NCBI website
