Monosomy 5p and trisomy 12p in a boy with familial balanced translocation

Clin Dysmorphol. 2006 Apr;15(2):85-7. doi: 10.1097/01.mcd.0000184971.69033.27.

Abstract

We report on a boy with monosomy 5p involving the Cri-du-Chat critical region and trisomy 12p detected by subtelomere study. Familial studies showed that the boy's mother and paternal grandfather had a balanced reciprocal translocation between the short arm of chromosomes 5 and 12. The boy had an overlap of features of both chromosomal conditions, even though the Cri-du-Chat phenotype was more prominent.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chromosomes, Human, Pair 12 / genetics*
  • Chromosomes, Human, Pair 5 / genetics*
  • Family
  • Female
  • Fingers / abnormalities
  • Foot Deformities, Congenital / complications
  • Foot Deformities, Congenital / genetics
  • Hand Deformities, Congenital / complications
  • Hand Deformities, Congenital / genetics
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Infant, Newborn
  • Male
  • Monosomy / genetics*
  • Syndactyly / complications
  • Translocation, Genetic*
  • Trisomy / genetics*