Structured Summary
Abstract
Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRANIOFACIAL ABNORMALITIES; digital malformations, and growth retardation.
MeSH Record
Classification
Broader headings
Related Concepts
Knowledge Graph
Drag nodes to rearrange; hover to trace links; click a node to open its page.
MeSH Record
Synonyms
4 entry terms
- Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum
- Acrocallosal Syndromes
- Syndrome, Acrocallosal
- Syndromes, Acrocallosal
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2009
MeSH Record
Previous Indexing
- Congenital Abnormalities (1963-2008)
- Corpus Callosum (1963-2008)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Acrocallosal Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D055673. http://id.nlm.nih.gov/mesh/2026/D055673
- Acrocallosal Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Acrocallosal_syndrome
- Acrocallosal Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q4675304