 Aicardi Syndrome
"Aicardi Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D058540
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| MeSH 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
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| Concept/Terms |
Aicardi Syndrome- Aicardi Syndrome
- Syndrome, Aicardi
- Corpus Callosum, Agenesis Of, With Chorioretinal Abnormality
- Chorioretinal Anomalies with Acc
- Agenesis of Corpus Callosum with Infantile Spasms and Ocular Abnormalities
- Callosal Agenesis and Ocular Abnormalities
- Aicardi's Syndrome
- Syndrome, Aicardi's
- Agenesis of Corpus Callosum with Chorioretinal Abnormality
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Below are MeSH descriptors whose meaning is more general than "Aicardi Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Aicardi Syndrome".
This graph shows the total number of publications written about "Aicardi Syndrome" by people in this website by year, and whether "Aicardi Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Aicardi Syndrome" by people in Profiles.
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Ha TT, Burgess R, Newman M, Moey C, Mandelstam SA, Gardner AE, Ivancevic AM, Pham D, Kumar R, Smith N, Patel C, Malone S, Ryan MM, Calvert S, van Eyk CL, Lardelli M, Berkovic SF, Leventer RJ, Richards LJ, Scheffer IE, Gecz J, Corbett MA. Aicardi Syndrome Is a Genetically Heterogeneous Disorder. Genes (Basel). 2023 07 31; 14(8).
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People  People who have written about this concept. _
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