Literature DB >> 1682494

Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis.

A H Bröcker-Vriends1, F R Rosendaal, J C van Houwelingen, E Bakker, G J van Ommen, J J van de Kamp, E Briët.   

Abstract

Coagulation and RFLP data from 41 families with an isolated haemophilia A patient were used to estimate the sex ratio of mutation frequencies (nu/mu). Based on the results of coagulation assays in all the female relatives investigated, nu/mu was estimated to be 12.1 by the maximum likelihood method (95% confidence interval 3.8 to 62.5). In order to avoid the possible influence of germline mosaicism, an additional analysis was performed in which only the results in the mothers and grandmothers of an isolated patient were included. The nu/mu ratio was then estimated to be 5.2 (95% confidence interval 1.8 to 15.1). Because an estimate of nu/mu based on all available RFLP data can easily be biased in favour of males, we set up a model in which only information on the grandparental derivation of the patient's X chromosome was used, irrespective of the generation in which the mutation actually occurred. In this way nu/mu was estimated to be minimally 4. The probability of carriership for mothers of an isolated haemophilia A patient amounts to 86% with a sex ratio of 5.2. Although this would imply that 14% of the mothers are not carriers of the disease in the classical sense, they may be mosaic for the mutation and, therefore, also at risk of transmitting the mutation more than once.

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Year:  1991        PMID: 1682494      PMCID: PMC1017053          DOI: 10.1136/jmg.28.10.672

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  46 in total

1.  Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations.

Authors:  E Bakker; H Veenema; J T Den Dunnen; C van Broeckhoven; P M Grootscholten; E J Bonten; G J van Ommen; P L Pearson
Journal:  J Med Genet       Date:  1989-09       Impact factor: 6.318

2.  First trimester prenatal diagnosis of haemophilia A: two years' experience.

Authors:  A H Bröcker-Vriends; E Briët; H H Kanhai; E Bakker; J C Dreesen; N J Leschot; J J Van de Kamp; P L Pearson
Journal:  Prenat Diagn       Date:  1988-07       Impact factor: 3.050

3.  Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.

Authors:  J T Den Dunnen; P M Grootscholten; E Bakker; L A Blonden; H B Ginjaar; M C Wapenaar; H M van Paassen; C van Broeckhoven; P L Pearson; G J van Ommen
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

4.  Ascertainment bias and power of procedures to estimate differences between male and female mutation rates.

Authors:  G J te Meerman; E R Karel; L P ten Kate
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132

5.  Molecular defects in hemophilia A: identification and characterization of mutations in the factor VIII gene and family analysis.

Authors:  M Higuchi; L Kochhan; R Schwaab; H Egli; H H Brackmann; J Horst; K Olek
Journal:  Blood       Date:  1989-08-15       Impact factor: 22.113

6.  Partial deletions of factor VIII gene as molecular diagnostic markers in haemophilia A.

Authors:  M Wehnert; F H Herrmann; K Wulff
Journal:  Dis Markers       Date:  1989 Apr-Jun       Impact factor: 3.434

7.  Sex ratio of the mutation frequencies in haemophilia A: estimation and meta-analysis.

Authors:  F R Rosendaal; A H Bröcker-Vriends; J C van Houwelingen; C Smit; I Varekamp; H van Dijck; T P Suurmeijer; J P Vandenbroucke; E Briët
Journal:  Hum Genet       Date:  1990-12       Impact factor: 4.132

8.  Modern haemophilia treatment: medical improvements and quality of life.

Authors:  F R Rosendaal; C Smit; I Varekamp; A H Bröcker-Vriends; H van Dijck; T P Suurmeijer; J P Vandenbroucke; E Briët
Journal:  J Intern Med       Date:  1990-12       Impact factor: 8.989

9.  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

10.  The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

Authors:  M Koenig; A H Beggs; M Moyer; S Scherpf; K Heindrich; T Bettecken; G Meng; C R Müller; M Lindlöf; H Kaariainen; A de la Chapellet; A Kiuru; M L Savontaus; H Gilgenkrantz; D Récan; J Chelly; J C Kaplan; A E Covone; N Archidiacono; G Romeo; S Liechti-Gailati; V Schneider; S Braga; H Moser; B T Darras; P Murphy; U Francke; J D Chen; G Morgan; M Denton; C R Greenberg; K Wrogemann; L A Blonden; M B van Paassen; G J van Ommen; L M Kunkel
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

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  8 in total

1.  High male:female ratio of germ-line mutations: an alternative explanation for postulated gestational lethality in males in X-linked dominant disorders.

Authors:  G H Thomas
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

2.  Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies.

Authors:  J Becker; R Schwaab; A Möller-Taube; U Schwaab; W Schmidt; H H Brackmann; T Grimm; K Olek; J Oldenburg
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

3.  Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene: a European study.

Authors:  A J van Essen; S Abbs; M Baiget; E Bakker; C Boileau; C van Broeckhoven; K Bushby; A Clarke; M Claustres; A E Covone
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

4.  Birth and population prevalence of Duchenne muscular dystrophy in The Netherlands.

Authors:  A J van Essen; H F Busch; G J te Meerman; L P ten Kate
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

Review 5.  The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B.

Authors:  A H Bröcker-Vriends; E Bakker; H H Kanhai; G J van Ommen; P H Reitsma; J J van de Kamp; E Briët
Journal:  Ann Hematol       Date:  1992-01       Impact factor: 3.673

6.  Constitutional and mosaic large NF1 gene deletions in neurofibromatosis type 1.

Authors:  S A Rasmussen; S D Colman; V T Ho; C R Abernathy; P H Arn; L Weiss; C Schwartz; R A Saul; M R Wallace
Journal:  J Med Genet       Date:  1998-06       Impact factor: 6.318

7.  On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis.

Authors:  T Grimm; G Meng; S Liechti-Gallati; T Bettecken; C R Müller; B Müller
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

8.  Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia A.

Authors:  J Oldenburg; R Schwaab; T Grimm; K Zerres; P Hakenberg; H H Brackmann; K Olek
Journal:  Am J Hum Genet       Date:  1993-12       Impact factor: 11.025

  8 in total

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