"Acrocallosal 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.
Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRANIOFACIAL ABNORMALITIES; digital malformations, and growth retardation.
| Descriptor ID |
D055673
|
| MeSH Number(s) |
C10.500.034.500 C16.131.666.034.500
|
| Concept/Terms |
Acrocallosal Syndrome- Acrocallosal Syndrome
- Acrocallosal Syndromes
- Syndrome, Acrocallosal
- Syndromes, Acrocallosal
- Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum
|
Below are MeSH descriptors whose meaning is more general than "Acrocallosal Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Acrocallosal Syndrome".
This graph shows the total number of publications written about "Acrocallosal Syndrome" by people in this website by year, and whether "Acrocallosal Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
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Below are the most recent publications written about "Acrocallosal Syndrome" by people in Profiles.
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Corpus callosum agenesis, severe mental retardation, epilepsy, and dyskinetic quadriparesis due to a novel mutation in the homeodomain of ARX. Am J Med Genet A. 2011 Apr; 155A(4):892-7.
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Agenesis of the corpus callosum and congenital lymphedema: A novel recognizable syndrome? Am J Med Genet A. 2010 Jul; 152A(7):1621-6.