Familial translocation (X;3) (p22.3;p23): chromosomal in situ suppression (CISS) hybridization and inactivation pattern study

Clin Genet. 1994 Nov;46(5):360-3. doi: 10.1111/j.1399-0004.1994.tb04179.x.

Abstract

High-resolution chromosome banding and chromosomal in situ suppression hybridization were used to identify a derivative X in a 10-month-old female patient with congenital heart defect and slight dysmorphism. The unbalanced karyotype was monosomic for Xp22.3-pter and trisomic for 3p23-pter regions. The derivative X was inherited from the mother carrier of a balanced translocation (X;3) (p22.3;p23). Replication study of the patient showed the abnormal X,t(X;3) to be late replicating, except for the translocated segment. This patient demonstrated only epicanthus and congenital heart defect, despite her partial trisomy 3. The clinical phenotype may be less severe when the X-chromosome is involved in an unbalanced translocation.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Cells, Cultured
  • Chromosome Banding
  • Chromosomes, Human, Pair 3*
  • Dosage Compensation, Genetic
  • Female
  • Fibroblasts / cytology
  • Humans
  • In Situ Hybridization / methods
  • Infant
  • Karyotyping
  • Leukocytes, Mononuclear / cytology
  • Male
  • Translocation, Genetic*
  • X Chromosome*