Interstitial deletion (6)q13q15

Am J Med Genet. 1996 Apr 24;62(4):345-7. doi: 10.1002/(SICI)1096-8628(19960424)62:4<345::AID-AJMG4>3.0.CO;2-Q.

Abstract

We report on a 2-year-old child with psychomotor retardation, facial and urogenital anomalies. His chromosome constitution was 46,XY, del(6)(q13q15). This case further contributes to the karyotype-phenotype correlation of proximal deletion 6q syndromes.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adult
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 6*
  • Face / abnormalities
  • Female
  • Humans
  • Intellectual Disability / genetics
  • Male
  • Urogenital Abnormalities