Literature DB >> 1637670

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

G J Draper1, B M Sanders, P A Brownbill, M M Hawkins.   

Abstract

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.

Entities:  

Mesh:

Year:  1992        PMID: 1637670      PMCID: PMC1977909          DOI: 10.1038/bjc.1992.244

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  22 in total

1.  [Genetic study of retinoblastoma (author's transl)].

Authors:  M L Briard-Guillemot; C Bonaïti-Pellié; J Feingold; J Frézal
Journal:  Humangenetik       Date:  1974

2.  Retinoblastoma. A review of ten years.

Authors:  N Leelawongs; C D Regan
Journal:  Am J Ophthalmol       Date:  1968-12       Impact factor: 5.258

3.  Retinoblastoma: a prototypic hereditary neoplasm.

Authors:  A G Knudson
Journal:  Semin Oncol       Date:  1978-03       Impact factor: 4.929

4.  The heredity of retinoblastoma.

Authors:  J Schappert-Kimmijser; G D Hemmes; R Nijland
Journal:  Ophthalmologica       Date:  1966       Impact factor: 3.250

5.  Mutation theory of carcinogenesis in retinoblastoma.

Authors:  C Bonaïti-Pellie; M L Briard-Guillemot; J Feingold; J Frezal
Journal:  J Natl Cancer Inst       Date:  1976-08       Impact factor: 13.506

Review 6.  Retinoblastoma: clues to human oncogenesis.

Authors:  A L Murphree; W F Benedict
Journal:  Science       Date:  1984-03-09       Impact factor: 47.728

7.  Retinoblastoma in Great Britain 1969-80: incidence, treatment, and survival.

Authors:  B M Sanders; G J Draper; J E Kingston
Journal:  Br J Ophthalmol       Date:  1988-08       Impact factor: 4.638

Review 8.  Genetics of retinoblastoma.

Authors:  F Vogel
Journal:  Hum Genet       Date:  1979-11-01       Impact factor: 4.132

Review 9.  The genetics of retinoblastoma.

Authors:  J K Cowell
Journal:  Br J Cancer       Date:  1991-03       Impact factor: 7.640

10.  Design and analysis of randomized clinical trials requiring prolonged observation of each patient. I. Introduction and design.

Authors:  R Peto; M C Pike; P Armitage; N E Breslow; D R Cox; S V Howard; N Mantel; K McPherson; J Peto; P G Smith
Journal:  Br J Cancer       Date:  1976-12       Impact factor: 7.640

View more
  37 in total

1.  New RB1 oncogenic mutations and intronic polymorphisms in Serbian retinoblastoma patients: genetic counseling implications.

Authors:  Milica Kontic; Iciar Palacios; Ángelo Gámez; Isabel Camino; Zoran Latkovic; Dejan Rasic; Vera Krstic; Vera Bunjevacki; Javier Alonso; Ángel Pestaña
Journal:  J Hum Genet       Date:  2006-09-14       Impact factor: 3.172

2.  Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.

Authors:  D R Lohmann; M Gerick; B Brandt; U Oelschläger; B Lorenz; E Passarge; B Horsthemke
Journal:  Am J Hum Genet       Date:  1997-08       Impact factor: 11.025

3.  Developmental stage-specific proliferation and retinoblastoma genesis in RB-deficient human but not mouse cone precursors.

Authors:  Hardeep P Singh; Sijia Wang; Kevin Stachelek; Sunhye Lee; Mark W Reid; Matthew E Thornton; Cheryl Mae Craft; Brendan H Grubbs; David Cobrinik
Journal:  Proc Natl Acad Sci U S A       Date:  2018-09-13       Impact factor: 11.205

4.  Differential diagnosis of type 2 neurofibromatosis: molecular discrimination of NF2 and sporadic vestibular schwannomas.

Authors:  C L Wu; N Thakker; W Neary; G Black; R Lye; R T Ramsden; A P Read; D G Evans
Journal:  J Med Genet       Date:  1998-12       Impact factor: 6.318

5.  Cost comparison of molecular versus conventional screening of relatives at risk for retinoblastoma.

Authors:  H Z Noorani; H N Khan; B L Gallie; A S Detsky
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

6.  Predictive testing for retinoblastoma comes of age.

Authors:  B L Gallie
Journal:  Am J Hum Genet       Date:  1997-08       Impact factor: 11.025

7.  Residential Pesticide Exposures in Pregnancy and the Risk of Sporadic Retinoblastoma: A Report From the Children's Oncology Group.

Authors:  Negar Omidakhsh; Arupa Ganguly; Greta R Bunin; Ondine S von Ehrenstein; Beate Ritz; Julia E Heck
Journal:  Am J Ophthalmol       Date:  2017-01-26       Impact factor: 5.258

8.  Retinoblastoma and low level radiation.

Authors:  C A Stiller
Journal:  BMJ       Date:  1993-08-21

9.  Radiographic findings in 13q-syndrome.

Authors:  S C Kaste; C B Pratt
Journal:  Pediatr Radiol       Date:  1993

Review 10.  Cancer of childhood in sub-Saharan Africa.

Authors:  Cristina Stefan; Freddie Bray; Jacques Ferlay; Biying Liu; D Maxwell Parkin
Journal:  Ecancermedicalscience       Date:  2017-07-28
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.