LGMD2I in a North American population.

Program in Genomics, Children's Hospital Boston and Harvard Medical School, Boston, USA. peter.kang@childrens.harvard.edu

BACKGROUND: There is a marked variation in clinical phenotypes that have been associated with mutations in FKRP, ranging from severe congenital muscular dystrophies to limb-girdle muscular dystrophy type 2I (LGMD2I). METHODS: We screened the FKRP gene in two cohorts totaling 87 patients with the LGMD phenotype. RESULTS: The c.826C>A, p.L276I mutation was present in six patients and a compound heterozygote mutation in a seventh patient. Six patients had a mild LGMD2I phenotype, which resembles that of Becker muscular dystrophy. The other patient had onset before the age of 3 years, and thus may follow a more severe course. CONCLUSION: These findings suggest that LGMD2I may be common in certain North American populations. This diagnosis should be considered early in the evaluation of LGMD.

PMID: 18036232 [PubMed - indexed for MEDLINE]

PMCID: PMC2216011