Aicardi Syndrome

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.

Year introduced: 2011

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Restrict to MeSH Major Topic.

Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C10.500.034.687, C11.270.019, C16.131.162, C16.131.666.034.687, C16.320.290.019, C16.320.322.030

MeSH Unique ID: D058540

Entry Terms:

• Syndrome, Aicardi
• Corpus Callosum, Agenesis Of, With Chorioretinal Abnormality
• Aicardi's Syndrome
• Syndrome, Aicardi's
• Agenesis of Corpus Callosum with Infantile Spasms and Ocular Abnormalities
• Callosal Agenesis and Ocular Abnormalities
• Chorioretinal Anomalies with Acc
• Agenesis of Corpus Callosum with Chorioretinal Abnormality

Previous Indexing:

• Syndrome (1972-2010)

All MeSH Categories
Diseases Category
Nervous System Diseases
Nervous System Malformations
Agenesis of Corpus Callosum
Aicardi Syndrome

All MeSH Categories
Diseases Category
Eye Diseases
Eye Diseases, Hereditary
Aicardi Syndrome

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Aicardi Syndrome

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Agenesis of Corpus Callosum
Aicardi Syndrome

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Aicardi Syndrome

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Aicardi Syndrome