Literature DB >> 2338336

Segregation analysis of 1885 DMD families: significant departure from the expected proportion of sporadic cases.

G Barbujani1, A Russo, G A Danieli, A W Spiegler, J Borkowska, I H Petrusewicz.   

Abstract

The proportion of sporadic cases of Duchenne muscular dystrophy has been estimated by classical segregation analysis in a pooled sample of 1885 sibships from 7 different countries. A significant departure from the theoretical expectations based on mutation-selection equilibrium is observed (segregation frequency = 0.439 +/- 0.017; frequency of sporadic cases = 0.229 +/- 0.026, at the maximum likelihood). The occurrence of germinal mosaicism in some of the mothers of Duchenne cases may account for this peculiar finding, although a possible role of inequality of mutation rates in the two sexes cannot be ruled out.

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Year:  1990        PMID: 2338336     DOI: 10.1007/bf00210802

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  19 in total

1.  Genetic tests under incomplete ascertainment.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1959-03       Impact factor: 11.025

2.  Formal genetics of muscular dystrophy.

Authors:  N E MORTON; C S CHUNG
Journal:  Am J Hum Genet       Date:  1959-12       Impact factor: 11.025

Review 3.  Review and hypotheses: somatic mosaicism: observations related to clinical genetics.

Authors:  J G Hall
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

4.  Complex segregation analysis and computer-assisted genetic risk assessment for Duchenne muscular dystrophy.

Authors:  W R Williams; M W Thompson; N E Morton
Journal:  Am J Med Genet       Date:  1983-02

5.  Duchenne muscular dystrophy: data from family studies.

Authors:  G A Danieli; M L Mostacciuolo; G Pilotto; C Angelini; A Bonfante
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

6.  RFLP analysis in families with sporadic hemophilia A. Estimate of the mutation ratio in male and female gametes.

Authors:  F Bernardi; G Marchetti; V Bertagnolo; L Faggioli; S Volinia; P Patracchini; S Bartolai; F Vannini; L Felloni; L Rossi
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

7.  A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male.

Authors:  B T Darras; U Francke
Journal:  Nature       Date:  1987 Oct 8-14       Impact factor: 49.962

8.  The genetic status of mothers of isolated cases of Duchenne muscular dystrophy.

Authors:  R J Lane; M Robinow; A D Roses
Journal:  J Med Genet       Date:  1983-02       Impact factor: 6.318

9.  Genetic epidemiology of Duchenne muscular dystrophy in Japan: classical segregation analysis.

Authors:  M Kanamori; N E Morton; K Fujiki; K Kondo
Journal:  Genet Epidemiol       Date:  1987       Impact factor: 2.135

10.  No sex difference in mutations rates of Duchenne muscular dystrophy.

Authors:  N Yasuda; K Kondô
Journal:  J Med Genet       Date:  1980-04       Impact factor: 6.318

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  15 in total

1.  Theoretical considerations on germline mosaicism in Duchenne muscular dystrophy.

Authors:  T Grimm; B Müller; C R Müller; M Janka
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

Review 2.  The muscular dystrophies: from genes to therapies.

Authors:  Richard M Lovering; Neil C Porter; Robert J Bloch
Journal:  Phys Ther       Date:  2005-12

3.  Estimation of the male and female mutation rates in Duchenne muscular dystrophy (DMD).

Authors:  B Müller; C Dechant; G Meng; S Liechti-Gallati; R A Doherty; J F Hejtmancik; E Bakker; A P Read; M Jeanpierre; K H Fischbeck
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

Review 4.  Dystrophin-deficient large animal models: translational research and exon skipping.

Authors:  Xinran Yu; Bo Bao; Yusuke Echigoya; Toshifumi Yokota
Journal:  Am J Transl Res       Date:  2015-08-15       Impact factor: 4.060

5.  The role of polymorphic short tandem (CA)n repeat loci segregation analysis in the detection of Duchenne muscular dystrophy carriers and prenatal diagnosis.

Authors:  Veronica Ferreiro; Florencia Giliberto; Liliana Francipane; Irene Szijan
Journal:  Mol Diagn       Date:  2005

6.  Detection of germline mosaicism in two Duchenne muscular dystrophy families using polymorphic dinucleotide (CA)n repeat loci within the dystrophin gene.

Authors:  Verónica Ferreiro; Irene Szijan; Florencia Giliberto
Journal:  Mol Diagn       Date:  2004

7.  Molecular genetic analysis of 67 patients with Duchenne/Becker muscular dystrophy.

Authors:  S Niemann-Seyde; R Slomski; F Rininsland; U Ellermeyer; J Kwiatkowska; J Reiss
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

8.  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

9.  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

10.  CUGC for Duchenne muscular dystrophy (DMD).

Authors:  David J Coote; Mark R Davis; Macarena Cabrera; Merrilee Needham; Nigel G Laing; Kristen J Nowak
Journal:  Eur J Hum Genet       Date:  2018-01-12       Impact factor: 4.246

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