Literature DB >> 1570845

Germinal mosaicism and risk calculation in X-linked diseases.

M Jeanpierre1.   

Abstract

Germinal mosaicism is a major problem in risk estimation for an X-linked disease. A mutation can happen anytime in germ cell development, and the proportion of germ cells bearing the mutated gene is twice the probability of recurrence of the mutation. This proportion could be either very low in late mutations or very high in germinal and somatic mosaicism. When this heterogeneity is taken into consideration, the distribution of the recurrence risk is conveniently represented as a set of discrete classes that may be derived either from models of gametogenesis or from empirical data. A computer program taking into account germinal mosaicism has been devised to calculate the probability of a possible carrier belonging to any of these classes, in order to settle the origin of the mutation of a given family. Germinal mosaicism increases the probability of inheriting the mutation, but this effect is always lowered by the possibility of heterogeneity. When the mother of a possible carrier is not herself a carrier, the risk of her daughter being a carrier is approximately halved, even under the assumption of a high recurrence risk from mosaicism.

Entities:  

Mesh:

Year:  1992        PMID: 1570845      PMCID: PMC1682604     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  32 in total

1.  Mutations of Bacteria from Virus Sensitivity to Virus Resistance.

Authors:  S E Luria; M Delbrück
Journal:  Genetics       Date:  1943-11       Impact factor: 4.562

2.  Mutational Mosaic Coat Patterns of the Guinea Pig.

Authors:  S Wright; O N Eaton
Journal:  Genetics       Date:  1926-07       Impact factor: 4.562

3.  The population genetics of Duchenne: natural and artificial selection in Duchenne muscular dystrophy.

Authors:  J H Edwards
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

4.  Achondroplasia in two sisters with normal parents.

Authors:  P Bowen
Journal:  Birth Defects Orig Artic Ser       Date:  1974

5.  Recurrence risks for germinal mosaics.

Authors:  D L Hartl
Journal:  Am J Hum Genet       Date:  1971-03       Impact factor: 11.025

6.  Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.

Authors:  A P Monaco; C J Bertelson; C Colletti-Feener; L M Kunkel
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132

7.  Germinal mosaicism in achondroplasia: a family with 3 affected siblings of normal parents.

Authors:  J P Fryns; A Kleczkowska; H Verresen; H van den Berghe
Journal:  Clin Genet       Date:  1983-09       Impact factor: 4.438

8.  Achondroplasia in sibs of normal parents.

Authors:  N Philip; M Auger; J F Mattei; F Giraud
Journal:  J Med Genet       Date:  1988-12       Impact factor: 6.318

9.  Achondroplasia: unexpected familial recurrence.

Authors:  C A Reiser; R M Pauli; J G Hall
Journal:  Am J Med Genet       Date:  1984-10

10.  Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy families.

Authors:  C R Müller; T Grimm
Journal:  Hum Genet       Date:  1986-10       Impact factor: 4.132

View more
  3 in total

1.  Genetic linkage analysis in the presence of germline mosaicism.

Authors:  Omer Weissbrod; Dan Geiger
Journal:  Stat Appl Genet Mol Biol       Date:  2011-10-04

2.  Recurrence risk for germinal mosaics revisited.

Authors:  M A van der Meulen; M J van der Meulen; G J te Meerman
Journal:  J Med Genet       Date:  1995-02       Impact factor: 6.318

3.  Nature and recurrence of AVPR2 mutations in X-linked nephrogenic diabetes insipidus.

Authors:  D G Bichet; M Birnbaumer; M Lonergan; M F Arthus; W Rosenthal; P Goodyer; H Nivet; S Benoit; P Giampietro; S Simonetti
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.