NirvanamKnowledge · Cases · Solver

Syndrome

Aicardi Syndrome

AMW:DIS:100378

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.

Pathology clinical
Read knowledge page ↗ Open graph Embed card

Graph assertions

Aicardi Syndrome has parent Agenesis of Corpus Callosum
Aicardi Syndrome has parent Congenital Abnormalities
Aicardi Syndrome has parent Eye Diseases, Hereditary
Aicardi Syndrome has parent Genetic Diseases, X-Linked

Embed this node