Possible inactivation of part of chromosome 13 due to 13qXp translocation associated with retinoblastoma

Clin Genet. 1982 Jun;21(6):357-61. doi: 10.1111/j.1399-0004.1982.tb01387.x.

Abstract

Chromosome examination of a female patient with 13/X translocation associated with retinoblastoma was carried out using peripheral blood lymphocytes and cultured skin fibroblasts. The constitutional karyotype was 46,X,t(13;X) (q12;p22). Q-banding analysis showed that the translocated chromosomes were of paternal origin. Studies on DNA replication pattern with Giemsa banding using the bromodeoxyuridine substitution technique revealed that the derivative X chromosome was late replicating, and the translocated chromosome 13 was affected by the spreading of lyonization. Such a functional monosomy of 13q14 may also be involved in retinal blasts, and be related to the development of retinoblastoma.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Banding
  • Chromosomes, Human, 13-15*
  • DNA Replication
  • Dosage Compensation, Genetic
  • Eye Neoplasms / genetics*
  • Female
  • Fibroblasts / ultrastructure
  • Humans
  • Infant
  • Karyotyping
  • Lymphocytes / ultrastructure
  • Retinoblastoma / genetics*
  • Sex Chromosomes*
  • Translocation, Genetic*
  • X Chromosome*