A 15-year molecular analysis of DMD/BMD: Genetic features in a large cohort

Antonella Carsana, Giulia Frisso, Mariano Intrieri, Maria Roberta Tremolaterra, Giovanni Savarese, Giovanni Scapagnini, Gabriella Esposito, Lucio Santoro, Francesco Salvatore

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Duchenne (DMD) and Becker muscular dystrophies (BMD) are X-linked recessive neuromuscular disorders caused by mutations in the dystrophin gene. In most cohorts, DMD/BMD are due to deletions (60-80%) and duplications (6-10%) involving one or more exons. The remaining cases are caused by different type of point mutations. We analyzed 179 unrelated male patients, 296 women belonging to 137 DMD/BMD families, and 93 independent patients referred for hyperCKemia. We identified 121 deletions and 11 duplications involving one or more exons and one complex rearrangement in the DMD/BMD patients, and 9 deletions in males referred for high levels of serum CK. Carrier status was investigated in 219 female relatives of deleted or duplicated DMD/BMD males, and by linkage analysis in 77 women belonging to families in which the causative mutation was not identified. Four carrier women with clinical manifestations of the disease had unbalanced X inactivation with a degree of X skewing between 70% and 93%. Large cohort studies from different geographic areas may be important for mutation typology comparisons and their appropriate analytical approach.

Original languageEnglish
Pages (from-to)547-558
Number of pages12
JournalFrontiers in Bioscience - Elite
Volume2 E
Issue number2
Publication statusPublished - Jan 1 2010

Fingerprint

Duchenne Muscular Dystrophy
Exons
Dystrophin
Genes
Mutation
X Chromosome Inactivation
Point Mutation
Cohort Studies
Serum

Keywords

  • Deletions
  • Duchenne/Becker muscular dystrophy
  • Duplications
  • Linkage analysis
  • MLPA
  • Noncontiguous duplications
  • Xinactivation

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Immunology and Microbiology(all)
  • Medicine(all)

Cite this

Carsana, A., Frisso, G., Intrieri, M., Tremolaterra, M. R., Savarese, G., Scapagnini, G., ... Salvatore, F. (2010). A 15-year molecular analysis of DMD/BMD: Genetic features in a large cohort. Frontiers in Bioscience - Elite, 2 E(2), 547-558.

A 15-year molecular analysis of DMD/BMD : Genetic features in a large cohort. / Carsana, Antonella; Frisso, Giulia; Intrieri, Mariano; Tremolaterra, Maria Roberta; Savarese, Giovanni; Scapagnini, Giovanni; Esposito, Gabriella; Santoro, Lucio; Salvatore, Francesco.

In: Frontiers in Bioscience - Elite, Vol. 2 E, No. 2, 01.01.2010, p. 547-558.

Research output: Contribution to journalArticle

Carsana, A, Frisso, G, Intrieri, M, Tremolaterra, MR, Savarese, G, Scapagnini, G, Esposito, G, Santoro, L & Salvatore, F 2010, 'A 15-year molecular analysis of DMD/BMD: Genetic features in a large cohort', Frontiers in Bioscience - Elite, vol. 2 E, no. 2, pp. 547-558.
Carsana A, Frisso G, Intrieri M, Tremolaterra MR, Savarese G, Scapagnini G et al. A 15-year molecular analysis of DMD/BMD: Genetic features in a large cohort. Frontiers in Bioscience - Elite. 2010 Jan 1;2 E(2):547-558.
Carsana, Antonella ; Frisso, Giulia ; Intrieri, Mariano ; Tremolaterra, Maria Roberta ; Savarese, Giovanni ; Scapagnini, Giovanni ; Esposito, Gabriella ; Santoro, Lucio ; Salvatore, Francesco. / A 15-year molecular analysis of DMD/BMD : Genetic features in a large cohort. In: Frontiers in Bioscience - Elite. 2010 ; Vol. 2 E, No. 2. pp. 547-558.
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