Neonatal death in cousins with trisomy 10q and monosomy 4p due to a familial translocation

Clin Genet. 1982 Dec;22(6):340-7. doi: 10.1111/j.1399-0004.1982.tb01850.x.

Abstract

Two cousins with trisomy for a part of the long arm of chromosome 10 and monosomy for the distal portion of the short arm of chromosome 4 are reported. These infants had severe, neonatally lethal multiple malformations. Certain of these malformations--including severe lower limb reductions, marked ophthalmologic anomalies and certain craniofacial features--are inconsistent with either a simple additive effect of the two component chromosomal anomalies, or chromosomal "epistasis" that would result in observing the phenotypic effect of only one of the chromosomal aberrations. Rather a synergistic effect of these two karyotypic anomalies has resulted in unique phenotypic features.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Aneuploidy
  • Chromosomes, Human, 4-5*
  • Chromosomes, Human, 6-12 and X*
  • Female
  • Humans
  • Infant, Newborn
  • Karyotyping
  • Male
  • Pedigree
  • Phenotype
  • Translocation, Genetic*
  • Trisomy*