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Becker muscular dystrophy presenting with complete heart block in the sixth decade

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Abstract

Becker muscular dystrophy may be associated with myocardial abnormalities which are usually diagnosed after the onset of weakness. We present a patient who developed complete heart block 6 years before the onset of muscle weakness which occurred unusually late at the age of 62 years.

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References

  1. Bushby K, Thambyaya M, Gardner-Medwin D (1991) Prevalence and incidence of Becker muscular dystrophy. Lancet 337: 1022–1024

    PubMed  Google Scholar 

  2. Darras BT (1990) Molecular genetics of Duchenne and Becker muscular dystrophy. J Paediatr 117: 1–15

    Google Scholar 

  3. Emery AEH, Skinner R (1976) Clinical studies in benign (Becker type) X linked muscular dystrophy. Clin Genet 10: 189–201

    PubMed  Google Scholar 

  4. Ringel SP, Carvoll JE, Schold C (1922) The spectrum of X linked recessive muscular dystrophy. Arch Neurol 34:408–516

    Google Scholar 

  5. Katlyer BC, Misra S, Somani PN, Chaterji AM (1977) Congestive cardiomyopathy in a family of Becker's X linked muscular dystrophy. Postgraduate Medical Journal, S3, pp 12–15

    Google Scholar 

  6. Levin R, Narahara K (1985) Right axis deviation and anterior wall thalium201 defect in Becker's muscular dystrophy. Am J Cardiol 56:203–204

    PubMed  Google Scholar 

  7. Casazzo F, Bambilla SG, Salvato A, Moraidi L, Gonda E, Bonacina E (1988) Cardiac transplantation in Becker muscular dystrophy. J Neurol 235:496–498

    PubMed  Google Scholar 

  8. Donofrio D, Challa V, Hackshaw B, Mills S, Cordwell R (1989) Cardiac transplantation in a patient with Becker muscular dystrophy and cardiomyopathy. Arch Neurol 46:705–707

    PubMed  Google Scholar 

  9. De Visser M, Voogt W de, La Riviere G (1992) The heart in Becker muscular dystrophy, fascioscapulohumeral dystrophy, and Bethlem myopathy. Muscle Nerve 15:591–596

    PubMed  Google Scholar 

  10. Nigro G, Limongelli FM, Guigliano M, Politano L, Passamano L, Stefanelli S (1983) Prospective study of X-linked progressive muscular dystrophy in Campania. Muscle Nerve 6:253–262

    PubMed  Google Scholar 

  11. Steare SE, Benatar A, Dubowitz V (1992) Subclinical cardiomyopathy in Becker muscular dystrophy. Br Heart J 68:304–308

    PubMed  Google Scholar 

  12. Merchut MP, Zdoncyk D, Gujrati M (1990) Cardiac transplantation in female Emery-Dreifuss muscular dystrophy. J Neurol 237:316–319

    PubMed  Google Scholar 

  13. Yoshioka M, Saida K, Itagaki Y, Kamiya T (1989) Follow up study of cardiac involvement in Emery-Dreifuss muscular dystrophy. Arch Dis Childh 64:713–715

    PubMed  Google Scholar 

  14. Ringel SP, Carvoll JE, Schold C (1977) The spectrum of X-linked recessive muscular dystrophy. Arch Neurol 34:408–416

    PubMed  Google Scholar 

  15. Sakata C, Sunohara N, Nonaka I, Arahata K, Sugita H (1990) A case of Becker muscular dystrophy presenting with cardiac failure as the initial symptom (in Japanese). Rinsho Shinkeigaku 30:210–213

    PubMed  Google Scholar 

  16. Gold R, Kress W, Meurers B, Meng G, Reichmann H, Muller C (1992) Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysis. Muscle Nerve 15:214–218

    PubMed  Google Scholar 

  17. Abbs S, Yau SC, Clark S, Mathew CG, Bobrow M (1991) A convenient multiplex PCR system for the detection of dystrophin deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods. J Med Genet 28:304–311

    PubMed  Google Scholar 

  18. Sunohara N, Arahata K, Hoffman EP, et al (1990) Quadriceps Myopathy: forme fruste of Becker muscular dystrophy. Ann Neurol 28:634–639

    PubMed  Google Scholar 

  19. Gospe SM, Lazarro RP, Laura NS, Grootscholter PM, Scott MO, Fischbeck KH (1989) Familial X linked myalgia and cramps. A nonprogressive myopathy associated with a deletion in the dystrophin gene. Neurology 39:1277–1280

    PubMed  Google Scholar 

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Quinlivan, R., Ball, J., Dunckley, M. et al. Becker muscular dystrophy presenting with complete heart block in the sixth decade. J Neurol 242, 398–400 (1995). https://doi.org/10.1007/BF00868396

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  • DOI: https://doi.org/10.1007/BF00868396

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