Complex translocation t(9;21)(9;22)(q12p13)(q12q11) in the family of a child with 9p trisomy syndrome

Hum Genet. 1976 Jul 7;33(1):73-6. doi: 10.1007/BF00447289.

Abstract

A case of partial trisomy 9 is described in a mentally retarded and dysmorphic child, confirming that this chromosome unbalance results in a characteristic clinical entity. This trisomy arose through aberrant segregation of translocation chromosome during meiosis in the patient's mother, who is a balanced heterozygote for a complex translocation involving chromosomes 9, 21 and 22. The phenotypically normal sister of the proposition is also carrier of the same complex translocation.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Chromosome Aberrations*
  • Chromosomes, Human, 21-22 and Y*
  • Chromosomes, Human, 6-12 and X*
  • Humans
  • Male
  • Pedigree
  • Phenotype
  • Translocation, Genetic*
  • Trisomy*