Related MeSH Hierarchy (6)
Diseases [C] » Nervous System Diseases [C10] » Nervous System Malformations » Agenesis of Corpus Callosum » Aicardi Syndrome
Diseases [C] » Eye Diseases [C11] » Eye Diseases, Hereditary » Aicardi Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Aicardi Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Nervous System Malformations » Agenesis of Corpus Callosum » Aicardi Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Eye Diseases, Hereditary » Aicardi Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Genetic Diseases, X-Linked » Aicardi Syndrome
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. MeSH
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Phase 2 Indicated Drugs (3)
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