Literature DB >> 3706399

Investigation on genetic heterogeneity in Duchenne muscular dystrophy.

E Rabbi-Bortolini, M Zatz.   

Abstract

The preliminary results of a study to investigate possible genetic heterogeneity in Duchenne muscular dystrophy (DMD) are reported. Ninety-eight patients have been analyzed: 47 were isolated cases; 51 were familial cases. The patients were divided into three groups (normal intelligence, borderline, and mentally retarded) according to mental capacity and a comparison of clinical evolution (onset of clinical signs and loss of ambulation) as well as serum enzyme activities (creatine-kinase and pyruvate-kinase). In addition intrafamilial correlation analysis was done for the same parameters. The preliminary results did not show a significant difference between DMD patients with normal intelligence and those with mental retardation.

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Year:  1986        PMID: 3706399     DOI: 10.1002/ajmg.1320240113

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


  2 in total

1.  Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy.

Authors:  S Hodgson; K Hart; S Abbs; J Heckmatt; E Rodillo; M Bobrow; V Dubowitz
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

2.  Cosegregation of schizophrenia with Becker muscular dystrophy: susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain?

Authors:  M Zatz; H Vallada; M S Melo; M R Passos-Bueno; A H Vieira; M Vainzof; M Gill; V Gentil
Journal:  J Med Genet       Date:  1993-02       Impact factor: 6.318

  2 in total

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