 Agenesis of Corpus Callosum
"Agenesis of Corpus Callosum" 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.
Birth defect that results in a partial or complete absence of the CORPUS CALLOSUM. It may be isolated or a part of a syndrome (e.g., AICARDI'S SYNDROME; ACROCALLOSAL SYNDROME; ANDERMANN SYNDROME; and HOLOPROSENCEPHALY). Clinical manifestations include neuromotor skill impairment and INTELLECTUAL DISABILITY of variable severity.
| Descriptor ID |
D061085
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| MeSH Number(s) |
C10.500.034 C16.131.666.034 C23.300.008
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| Concept/Terms |
Agenesis of Corpus Callosum- Agenesis of Corpus Callosum
- Corpus Callosum Ageneses
- Corpus Callosum Agenesis
- Ageneses, Corpus Callosum
- Agenesis, Corpus Callosum
- Corpus Callosum Hypogenesis
- Corpus Callosum Hypogeneses
- Hypogeneses, Corpus Callosum
- Hypogenesis, Corpus Callosum
- Corpus Callosum, Agenesis Of
- Absence of Corpus Callosum
- Corpus Callosum Absence
- Corpus Callosum Absences
- Corpus Callosum Dysgenesis
- Corpus Callosum Dysgeneses
- Dysgeneses, Corpus Callosum
- Dysgenesis, Corpus Callosum
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Below are MeSH descriptors whose meaning is more general than "Agenesis of Corpus Callosum".
Below are MeSH descriptors whose meaning is more specific than "Agenesis of Corpus Callosum".
This graph shows the total number of publications written about "Agenesis of Corpus Callosum" by people in UAMS Profiles by year, and whether "Agenesis of Corpus Callosum" 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 | 0 | 1 | 1 | | 2022 | 0 | 1 | 1 | | 2018 | 0 | 1 | 1 | | 2015 | 1 | 0 | 1 | | 2008 | 0 | 1 | 1 | | 2007 | 1 | 0 | 1 | | 1995 | 1 | 0 | 1 | | 1993 | 1 | 0 | 1 |
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Below are the most recent publications written about "Agenesis of Corpus Callosum" by people in Profiles over the past ten years.
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AlAbdi L, Desbois M, Rusnac DV, Sulaiman RA, Rosenfeld JA, Lalani S, Murdock DR, Burrage LC, Billie Au PY, Towner S, Wilson WG, Wong L, Brunet T, Strobl-Wildemann G, Burton JE, Hoganson G, McWalter K, Begtrup A, Zarate YA, Christensen EL, Opperman KJ, Giles AC, Helaby R, Kania A, Zheng N, Grill B, Alkuraya FS. Loss-of-function variants in MYCBP2 cause neurobehavioural phenotypes and corpus callosum defects. Brain. 2023 04 19; 146(4):1373-1387.
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Shwe WH, Schlatterer SD, Williams J, du Plessis AJ, Mulkey SB. Outcome of Agenesis of the Corpus Callosum Diagnosed by Fetal MRI. Pediatr Neurol. 2022 10; 135:44-51.
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Samanta D, Ramakrishnaiah R. Neuroimaging Findings in a Child With SensorineuralHearing Loss. Pediatr Neurol. 2018 11; 88:75-76.
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Samanta D. Severe developmental delay and complete agenesis of corpus callosum in a Noonan syndrome patient with SOS1 mutation. Acta Neurol Belg. 2016 Jun; 116(2):223-4.
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