Acrocallosal Syndrome

Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRANIOFACIAL ABNORMALITIES; digital malformations, and growth retardation.

Year introduced: 2009

PubMed search builder options

Subheadings:

Restrict to MeSH Major Topic.

Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C10.500.034.500, C16.131.666.034.500

MeSH Unique ID: D055673

Entry Terms:

• Acrocallosal Syndromes
• Syndrome, Acrocallosal
• Syndromes, Acrocallosal
• Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum

Previous Indexing:

• Congenital Abnormalities (1963-2008)
• Corpus Callosum (1963-2008)

All MeSH Categories
Diseases Category
Nervous System Diseases
Nervous System Malformations
Agenesis of Corpus Callosum
Acrocallosal Syndrome

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Agenesis of Corpus Callosum
Acrocallosal Syndrome