Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues

Clin Genet. 1997 Aug;52(2):126-9. doi: 10.1111/j.1399-0004.1997.tb02530.x.

Abstract

Partial trisomy 6p is regarded as a distinct phenotype with short stature, failure to thrive, facial dysmorphisms with blepharophimosis, mental retardation and other malformations. An 18-month-old girl with typical features of partial trisomy 6p showed a de novo unbalanced translocation resulting in partial trisomy 6p21 to pter and partial monosomy 18p11 to pter. The translocation was observed in all fibroblasts analyzed, but only in 6% of the peripheral lymphocytes.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics
  • Chromosome Aberrations / genetics*
  • Chromosome Disorders
  • Chromosomes, Human, Pair 6 / genetics*
  • Craniofacial Abnormalities / genetics
  • Female
  • Fibroblasts
  • Growth Disorders / genetics
  • Humans
  • Infant
  • Intellectual Disability / genetics
  • Lymphocytes
  • Monosomy / genetics
  • Mosaicism / genetics*
  • Phenotype
  • Skin / cytology
  • Translocation, Genetic / genetics*
  • Trisomy / genetics*