Facioscapulohumeral muscular dystrophy: Epidemiological and molecular study in a north-east Italian population sample

M. L. Mostacciuolo, E. Pastorello, G. Vazza, M. Miorin, C. Angelini, G. Tomelleri, G. Galluzzi, Carlo Pietro Trevisan

Research output: Contribution to journalArticlepeer-review


Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant disease associated with a partial deletion on chromosome 4q35. Few relevant investigations have been reported on its epidemiology and were essentially based on clinical diagnosis, having been performed before recognition of the molecular mutation. We report an epidemiological survey on FSHD patients, in which the diagnosis was obtained by combined clinical and molecular evaluation. The survey concerned the north-east Italian province of Padova, an area of 871,190 inhabitants (1 January 2004). We identified 40 patients affected by FSHD based on clinical diagnosis. In 33 of them, the EcoRI fragment size in the 4q35 region ranged from 14 to 35kb. Four other patients belonging to the same family harbored a 38-kb fragment. In these four cases, the relationship between the borderline deletion with the mild FSHD phenotype was corroborated by additional haplotype reconstruction and segregation analysis. Interestingly, the same mild facial-sparing clinical pattern was apparent only in one other patient with an EcoRI fragment of 32kb, suggesting that this unusual FSHD phenotype may be due to very small 4q35 deletions. On the whole, estimating a prevalence rate of 44×10 -6, our survey confirmed FSHD as one of the most frequent neuromuscular disorders in Western populations.

Original languageEnglish
Pages (from-to)550-555
Number of pages6
JournalClinical Genetics
Issue number6
Publication statusPublished - 2009


  • Dystrophy
  • Epidemiology
  • Facioscapulohumeral muscular
  • FSHD
  • Prevalence

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics


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