Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5

Am J Med Genet. 1992 Oct 1;44(3):356-60. doi: 10.1002/ajmg.1320440317.

Abstract

We report on a 3-generation family with an interstitial deletion of the short arm of chromosome 5. Varied manifestations were found among the affected individuals including microcephaly, hypertonia, and micrognathia; mental retardation was common to all affected individuals. High resolution chromosome analysis was interpreted as del(5) (pter- > p14.3::p13.3- > qter). Molecular comparison of the deletion in this family with individuals with other 5p deletions suggests that the clinical findings are due specifically to the chromosomal material deleted from 5p13.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Blotting, Southern
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 18
  • Chromosomes, Human, Pair 5*
  • DNA / analysis
  • Female
  • Humans
  • Hybrid Cells
  • Intellectual Disability / genetics
  • Male
  • Microcephaly / genetics
  • Muscle Hypertonia / genetics
  • Trisomy

Substances

  • DNA