Genetic heterogeneity of cebocephaly

J Med Genet. 1974 Mar;11(1):35-40. doi: 10.1136/jmg.11.1.35.

Abstract

Three infants with cebocephaly with entirely different aetiologies are described: one possibly representing the effect of a single mutant gene, one with apparent E trisomy, and one with D trisomy. In comparison with other reported patients, it is likely that infants with cebocephaly and no associated chromosomal abnormality have few, if any, extracranial malformations.

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Brain / abnormalities*
  • Chromosome Aberrations / genetics*
  • Chromosome Disorders
  • Chromosomes, Human, 13-15
  • Chromosomes, Human, 16-18
  • Face / abnormalities*
  • Female
  • Genes
  • Humans
  • Infant, Newborn
  • Karyotyping
  • Male
  • Micrognathism
  • Mutation
  • Trisomy