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
|
| MeSH Number(s) |
C10.500.034 C16.131.666.034 C23.300.008
|
| Concept/Terms |
Agenesis of Corpus Callosum- Agenesis of Corpus Callosum
- Corpus Callosum Ageneses
- Corpus Callosum, Agenesis Of
- Corpus Callosum Dysgenesis
- Corpus Callosum Dysgeneses
- Dysgeneses, Corpus Callosum
- Dysgenesis, Corpus Callosum
- Absence of Corpus Callosum
- Corpus Callosum Absence
- Corpus Callosum Absences
- Corpus Callosum Agenesis
- Ageneses, Corpus Callosum
- Agenesis, Corpus Callosum
- Corpus Callosum Hypogenesis
- Corpus Callosum Hypogeneses
- Hypogeneses, Corpus Callosum
- Hypogenesis, Corpus Callosum
|
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 this website by year, and whether "Agenesis of Corpus Callosum" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 5 | 1 | 6 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Agenesis of Corpus Callosum" by people in Profiles.
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Paroxysmal hypothermia and hyperhidrosis with exacerbation after COVID-19 Infection. Clin Auton Res. 2021 04; 31(2):327-329.
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Accuracy of prenatal ultrasound in the diagnosis of corpus callosum anomalies. J Matern Fetal Neonatal Med. 2021 Feb; 34(3):439-444.
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Corpus callosum agenesis and clinically isolated syndrome (CIS): A case report. Mult Scler Relat Disord. 2019 01; 27:342-343.
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Fetal midline anomalies: Diagnosis and counselling Part 1: Corpus callosum anomalies. Eur J Paediatr Neurol. 2018 Nov; 22(6):951-962.
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Etiology and Prognosis of Severe Ventriculomegaly Diagnosed at Late Gestation. Ultraschall Med. 2018 Dec; 39(6):675-689.
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Hypercalciuria and nephrolithiasis: Expanding the renal phenotype of Donnai-Barrow syndrome. Clin Genet. 2018 07; 94(1):187-188.
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Biallelic inactivating variants in the GTPBP2 gene cause a neurodevelopmental disorder with severe intellectual disability. Eur J Hum Genet. 2018 04; 26(4):592-598.
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The Vici syndrome protein EPG5 regulates intracellular nucleic acid trafficking linking autophagy to innate and adaptive immunity. Autophagy. 2018; 14(1):22-37.