Cargando…

Patterns of risk of hereditary retinoblastoma and applications to genetic counselling.

A registry including information about nearly 1,600 cases of retinoblastoma diagnosed in Britain has been created at the Childhood Cancer Research Group. Cases have been classified as 'old germ cell mutation', 'new germ cell mutation' or 'sporadic non-hereditary'. For a...

Descripción completa

Detalles Bibliográficos
Autores principales: Draper, G. J., Sanders, B. M., Brownbill, P. A., Hawkins, M. M.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1992
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977909/
https://www.ncbi.nlm.nih.gov/pubmed/1637670
_version_ 1782135363671687168
author Draper, G. J.
Sanders, B. M.
Brownbill, P. A.
Hawkins, M. M.
author_facet Draper, G. J.
Sanders, B. M.
Brownbill, P. A.
Hawkins, M. M.
author_sort Draper, G. J.
collection PubMed
description A registry including information about nearly 1,600 cases of retinoblastoma diagnosed in Britain has been created at the Childhood Cancer Research Group. Cases have been classified as 'old germ cell mutation', 'new germ cell mutation' or 'sporadic non-hereditary'. For a population-based group of 918 cases diagnosed between 1962 and 1985 we have calculated the proportions of unilateral/bilateral and hereditary/non-hereditary cases. Bilateral cases represent 40% of the total number over this period; the proportion known to be hereditary is 44%, a higher proportion than has been reported elsewhere. By following up selected groups of cases, an estimate has been made of the proportions of siblings of retinoblastoma patients and offspring of survivors from retinoblastoma who are themselves affected with the disease. Where there is no previous family history, the risk for siblings of retinoblastoma patients of developing the disease is approximately 2% if the disease in the affected child is bilateral and 1% if it is unilateral, assuming that there are no other siblings; if there are unaffected siblings the risks for subsequent children are lower. Children of patients with hereditary retinoblastoma have a one in two chance of carrying the germ cell mutation and for those who are carriers the probability of developing retinoblastoma is very close to the accepted figure of 90% if the parents have bilateral retinoblastoma but probably less if they have the unilateral form. For children of patients not known to be carriers, the probability of developing retinoblastoma is estimated to be about 1%, considerably lower than the previously accepted figure of about 5%. Retinoblastoma kindreds consist mainly of bilateral cases but there is evidence that some kindreds have a high proportion of unilateral cases. The ways in which these findings may be used in conjunction with modern techniques of molecular biology for prenatal and postnatal genetic counselling are discussed.
format Text
id pubmed-1977909
institution National Center for Biotechnology Information
language English
publishDate 1992
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-19779092009-09-10 Patterns of risk of hereditary retinoblastoma and applications to genetic counselling. Draper, G. J. Sanders, B. M. Brownbill, P. A. Hawkins, M. M. Br J Cancer Research Article A registry including information about nearly 1,600 cases of retinoblastoma diagnosed in Britain has been created at the Childhood Cancer Research Group. Cases have been classified as 'old germ cell mutation', 'new germ cell mutation' or 'sporadic non-hereditary'. For a population-based group of 918 cases diagnosed between 1962 and 1985 we have calculated the proportions of unilateral/bilateral and hereditary/non-hereditary cases. Bilateral cases represent 40% of the total number over this period; the proportion known to be hereditary is 44%, a higher proportion than has been reported elsewhere. By following up selected groups of cases, an estimate has been made of the proportions of siblings of retinoblastoma patients and offspring of survivors from retinoblastoma who are themselves affected with the disease. Where there is no previous family history, the risk for siblings of retinoblastoma patients of developing the disease is approximately 2% if the disease in the affected child is bilateral and 1% if it is unilateral, assuming that there are no other siblings; if there are unaffected siblings the risks for subsequent children are lower. Children of patients with hereditary retinoblastoma have a one in two chance of carrying the germ cell mutation and for those who are carriers the probability of developing retinoblastoma is very close to the accepted figure of 90% if the parents have bilateral retinoblastoma but probably less if they have the unilateral form. For children of patients not known to be carriers, the probability of developing retinoblastoma is estimated to be about 1%, considerably lower than the previously accepted figure of about 5%. Retinoblastoma kindreds consist mainly of bilateral cases but there is evidence that some kindreds have a high proportion of unilateral cases. The ways in which these findings may be used in conjunction with modern techniques of molecular biology for prenatal and postnatal genetic counselling are discussed. Nature Publishing Group 1992-07 /pmc/articles/PMC1977909/ /pubmed/1637670 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Draper, G. J.
Sanders, B. M.
Brownbill, P. A.
Hawkins, M. M.
Patterns of risk of hereditary retinoblastoma and applications to genetic counselling.
title Patterns of risk of hereditary retinoblastoma and applications to genetic counselling.
title_full Patterns of risk of hereditary retinoblastoma and applications to genetic counselling.
title_fullStr Patterns of risk of hereditary retinoblastoma and applications to genetic counselling.
title_full_unstemmed Patterns of risk of hereditary retinoblastoma and applications to genetic counselling.
title_short Patterns of risk of hereditary retinoblastoma and applications to genetic counselling.
title_sort patterns of risk of hereditary retinoblastoma and applications to genetic counselling.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977909/
https://www.ncbi.nlm.nih.gov/pubmed/1637670
work_keys_str_mv AT drapergj patternsofriskofhereditaryretinoblastomaandapplicationstogeneticcounselling
AT sandersbm patternsofriskofhereditaryretinoblastomaandapplicationstogeneticcounselling
AT brownbillpa patternsofriskofhereditaryretinoblastomaandapplicationstogeneticcounselling
AT hawkinsmm patternsofriskofhereditaryretinoblastomaandapplicationstogeneticcounselling