Trisomy 20q. A new case and further phenotypic delineation

Clin Genet. 1990 May;37(5):363-6. doi: 10.1111/j.1399-0004.1990.tb03520.x.

Abstract

The present report concerns the clinical and cytogenetic findings in a liveborn girl with trisomy for the long arm of chromosome 20. She was the unbalanced product of a maternal t(18;20)(q23.2;q13.1) translocation. Our case is compared to the 3 previous reports of trisomy 20q associated with telomeric translocation. Adenosine deaminase dosage falls in the normal range and confirms the exclusion of the ADA locus from the region extending distally to 20q13.1.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Chromosomes, Human, Pair 20 / ultrastructure*
  • Face / abnormalities*
  • Face / pathology
  • Female
  • Humans
  • Infant
  • Phenotype
  • Trisomy*