Becker Muscular Dystrophy in a Patient with Hodgkin's Disease

Stefano Cereda, Graziella Cefalo, Monica Terenziani, Serena Catania, Franca Fossati-Bellani

Research output: Contribution to journalArticlepeer-review


Genetic disease often predisposes to neoplastic processes because of either alterations in both oncogenes and tumor suppressor genes or imbalances in the cell cycle. The authors present the case of a 15-year-old boy with Hodgkin's disease associated with Becker muscular dystrophy. Becker muscular dystrophy is an X-linked neuromuscular disease due to in-frame mutations in the dystrophin gene, and it is considered a milder variant of Duchenne muscular dystrophy. In most patients with Becker muscular dystrophy, the myopathic process affects the myocardium, leading to cardiomyopathy.

Original languageEnglish
Pages (from-to)72-73
Number of pages2
JournalJournal of Pediatric Hematology/Oncology
Issue number1
Publication statusPublished - Jan 2004


  • Becker muscular dystrophy
  • Cardiomyopathy
  • Genetic disease
  • Hodgkin's disease

ASJC Scopus subject areas

  • Hematology
  • Oncology
  • Pediatrics, Perinatology, and Child Health


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