Duplication of 7p: further delineation of the phenotype and restriction of the critical region to the distal part of the short arm

Am J Med Genet. 1996 Jan 2;61(1):21-5. doi: 10.1002/(SICI)1096-8628(19960102)61:1<21::AID-AJMG4>3.0.CO;2-#.

Abstract

We report on a patient with duplication of 7p15-->pter and review the literature. Patients with partial duplication of the distal 7p, including only the distal segment 7p15-->pter, have a syndrome comparable to that of patients with a larger or complete duplication of 7p. This suggests that the critical region for the dup(7p) phenotype is restricted to 7p15-->pter. The complete clinical phenotype of dup(7)(p15-->pter) includes mental retardation, skull anomalies, large anterior fontanel, cardiovascular defects, joint dislocation and contraction, and gastrointestinal and genital defects. Recognition of the clinical spectrum in patients with a smaller duplication of 7p, and the assignment of this critical region, should prove valuable for accurate counseling, prediction of outcome, and further gene mapping.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Abnormalities, Multiple / diagnosis
  • Abnormalities, Multiple / genetics*
  • Adult
  • Brain / diagnostic imaging
  • Brain / pathology
  • Brain / physiopathology
  • Chromosome Aberrations*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 7*
  • Electroencephalography
  • Female
  • Humans
  • Infant
  • Intellectual Disability / genetics
  • Magnetic Resonance Imaging
  • Male
  • Phenotype
  • Tomography, X-Ray Computed