"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.
MeSH Number(s)
C10.500.034.500
C16.131.666.034.500
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 Harvard Catalyst Profiles by year, and whether "Acrocallosal Syndrome" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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2009 | 0 | 1 | 1 |
Below are the most recent publications written about "Acrocallosal Syndrome" by people in Profiles.
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KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes. Nat Genet. 2011 Jun; 43(6):601-6.
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Why schizophrenia epidemiology needs neurobiology--and vice versa. Schizophr Bull. 2009 May; 35(3):577-81.