Structured Summary
Abstract
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 Record
Classification
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MeSH Record
Synonyms
8 entry terms
- Agenesis of Corpus Callosum with Chorioretinal Abnormality
- Agenesis of Corpus Callosum with Infantile Spasms and Ocular Abnormalities
- Aicardi's Syndrome
- Callosal Agenesis and Ocular Abnormalities
- Chorioretinal Anomalies with Acc
- Corpus Callosum, Agenesis Of, With Chorioretinal Abnormality
- Syndrome, Aicardi
- Syndrome, Aicardi's
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2011
MeSH Record
Previous Indexing
- Syndrome (1972-2010)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Aicardi Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D058540. http://id.nlm.nih.gov/mesh/2026/D058540
- Aicardi Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Aicardi_syndrome
- Aicardi Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q403463