Partial monosomy of distal 10q: three new cases and a review

Am J Med Genet. 1999 Sep 3;86(1):1-5.

Abstract

We report on 3 patients with partial deletions of the long arm of chromosome 10-46,XY,del (10)(q26.2), 46,XX,del(10) (q25.3q26.3) or 46,XX,del(10)(q26.1), and 46,XX,del (10)(q26.1). They are compared with other known cases with interstitial or terminal deletions involving chromosome bands 10q25 or q26. Unique manifestations are identified, including scoliosis and a severe behavior disorder with attention deficit and hyperactivity in a 12-year-old boy as well as patchy alopecia in a 6-year-old patient.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Abnormalities, Multiple / genetics
  • Child
  • Chromosome Breakage / genetics
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 10 / genetics*
  • Female
  • Heart Diseases / congenital
  • Heart Diseases / genetics
  • Humans
  • Male
  • Monosomy / genetics*
  • Phenotype
  • Sex Differentiation / genetics