Literature DB >> 1849353

Familial occurrence of Duchenne dystrophy through paternal lines in four families.

M Zatz1, M R Passos-Bueno, D Rapaport, M Vainzof.   

Abstract

In a survey of 454 families with patients affected with Duchenne muscular dystrophy (DMD) we have found 4 genealogies with 2 or more affected patients who were related through paternal lines. In 1 of these families, 2 affected cousins showed different DNA deletions suggesting 2 independent mutations; in the other 2, in which only the propositus could be studied DNA deletions were also detected in the dystrophin gene. In the last one, with 3 affected patients, no DNA deletions were detected but immunohistochemical study of muscle biopsies showed a negative dystrophin pattern typical of DMD. Although one of these families might have occurred by chance, the probability of finding the other 3 in our sample of families with DMD patients constitutes a rare event. It is suggested that other mechanisms, such as the presence of transposable elements in other sites of the genome, could be responsible in some families, for a greater predisposition for the occurrence of pathogenic deletions, duplications or mutations.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1849353     DOI: 10.1002/ajmg.1320380118

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  2 in total

1.  Multiple mutation in an extended Duchenne muscular dystrophy family.

Authors:  A Miciak; A Keen; D Jadayel; S Bundey
Journal:  J Med Genet       Date:  1992-02       Impact factor: 6.318

2.  Racial distribution of Duchenne muscular dystrophy in the West Midlands region of Britain.

Authors:  A Roddie; S Bundey
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.