Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counseling

Klin Monbl Augenheilkd. 1996 May;208(5):400-3. doi: 10.1055/s-2008-1035252.

Abstract

Purpose and method: The parental origin of initial somatic and germline mutations (M1) in the retinoblastoma gene (RB1) was explored in 36 retinoblastoma (Rb) and 5 retinoma patients, of which 16 were presumably non-hereditary and 25 were hereditary. By this approach the male:female mutation ratio was determined by the gender quotient of mutation origin.

Results: The male to female mutation ratio in hereditary Rb was 19:2, which is consistent with a significant bias towards paternal origin of germline mutation. This ratio was of 5:2 in non-hereditary Rb which is not significant.

Discussion: Together with the published data, these results support a preferential paternal mutagenesis in hereditary Rb, but appear to reject paternal genomic imprinting at the RB1 locus as previously proposed in non-hereditary Rb. Genetic counseling in sporadic Rb may be substantially improved by the identification of the parental origin of initial mutation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cohort Studies
  • Eye Neoplasms / diagnosis
  • Eye Neoplasms / genetics*
  • Female
  • Genes, Retinoblastoma / genetics
  • Genetic Carrier Screening
  • Genetic Counseling*
  • Germ-Line Mutation / genetics*
  • Humans
  • Male
  • Pedigree
  • Retinoblastoma / diagnosis
  • Retinoblastoma / genetics*
  • Sex Chromosome Aberrations / diagnosis
  • Sex Chromosome Aberrations / genetics*