Acrocallosal Syndrome
Also known asAcrocallosal Syndromes · Syndrome, Acrocallosal · Syndromes, Acrocallosal · Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum
Definition
Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRANIOFACIAL ABNORMALITIES; digital malformations, and growth retardation.
MeSH classification
- C10.500.034.500
- C16.131.666.034.500
Need clinical context, treatments, or patient-language explanation?
Ask GoDavaii AI about Acrocallosal SyndromeRelated concepts
Agenesis of Corpus Callosum
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…
Aicardi Syndrome
A rare genetic disorder characterized by partial or complete absence of the CORPUS CALLOSUM, resulting in infantile spasms, MENTAL RETARDATI…
Common questions about Acrocallosal Syndrome
What does Acrocallosal Syndrome mean in medicine?
Is Acrocallosal Syndrome known by any other names?
Where does Acrocallosal Syndrome sit in the medical classification?
Where can I get a plain-language explanation of Acrocallosal Syndrome?
Source: NIH MeSH 2026 (D055673) — National Library of Medicine, public domain. View official MeSH record ↗