A paternally derived inverted duplication of 7q with evidence of a telomeric deletion

Am J Med Genet. 1997 Jan 10;68(1):76-81.

Abstract

We report on a de novo constitutional rearrangement involving the long arm of chromosome 7 in a second trimester fetus with the karyotype of 46,XX, inv dup del (7)(pter-q36::q36-q21.2:) pat. Both a large duplication (q21.2-q36) and a small deletion (within q36) were confirmed by FISH studies. DNA analysis on the family showed that the abnormal chromosome was derived from a single paternal homolog. A mechanism is proposed in light of this finding. The phenotype at autopsy was consistent with reported cases of similar duplications in chromosome 7 in that hydrocephalus, a depressed nasal bridge, low set ears, microretrognathia and a short neck were present.

MeSH terms

  • Abortion, Therapeutic*
  • Adult
  • Chromosome Aberrations / diagnosis*
  • Chromosome Disorders
  • Chromosome Inversion
  • Chromosomes, Human, Pair 7*
  • Female
  • Genomic Imprinting
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Male
  • Pregnancy