NIH MeSH · D055673Diseases

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

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Related concepts

Source: NIH MeSH 2026 (D055673) — National Library of Medicine, public domain. View official MeSH record ↗