Emerging phenotype of duplication (7p): a report of three cases and review of the literature

Am J Med Genet. 1989 Jul;33(3):364-8. doi: 10.1002/ajmg.1320330315.

Abstract

Here we report on three patients with dup (7p) and review the previously published 17 cases. Characteristic manifestations include severe/profound psychomotor retardation, dolichocephaly or microbrachycephaly, gaping fontanels and wide sagittal and metopic sutures, hypertelorism, large apparently low-set ears, micrognathia, choanal atresia/stenosis, hyperextensible joints subject to dislocation, joint contractures, and a high rate of cardiac septal defects. Our analysis suggests that dup(7p) is associated with a recognizable characteristic phenotype.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Chromosome Aberrations / genetics*
  • Chromosome Disorders
  • Chromosomes, Human, Pair 7*
  • Facial Bones / abnormalities
  • Female
  • Heart Defects, Congenital / genetics
  • Humans
  • Infant, Newborn
  • Intellectual Disability / genetics
  • Male
  • Multigene Family*
  • Psychomotor Disorders / genetics
  • Skull / abnormalities
  • Syndrome
  • Translocation, Genetic