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Durham Research Online
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Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C.

Brockington, M. and Yuva, Y. and Prandini, P. and Brown, S. C. and Torelli, S. and Benson, M. A. and Herrmann, R. and Anderson, L. V. B. and Bashir, R. and Burgunder, J. M. and Fallet, S. and Romero, N. and Fardeau, M. and Straub, V. and Storey, G. and Pollitt, C. and Richard, I. and Sewry, C. A. and Bushby, K. and Voit, T. and Blake, D. J. and Muntoni, F. (2001) 'Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C.', Human molecular genetics., 10 (25). pp. 2851-2859.

Abstract

The limb girdle and congenital muscular dystrophies (LGMD and CMD) are characterized by skeletal muscle weakness and dystrophic muscle changes. The onset of symptoms in CMD is within the first few months of life, whereas in LGMD they can occur in late childhood, adolescence or adult life. We have recently demonstrated that the fukutin-related protein gene (FKRP) is mutated in a severe form of CMD (MDC1C), characterized by the inability to walk, leg muscle hypertrophy and a secondary deficiency of laminin 2 and -dystroglycan. Both MDC1C and LGMD2I map to an identical region on chromosome 19q13.3. To investigate whether these are allelic disorders, we undertook mutation analysis of FKRP in 25 potential LGMD2I families, including some with a severe and early onset phenotype. Mutations were identified in individuals from 17 families. A variable reduction of -dystroglycan expression was observed in the skeletal muscle biopsy of all individuals studied. In addition, several cases showed a deficiency of laminin 2 either by immunocytochemistry or western blotting. Unexpectedly, affected individuals from 15 families had an identical C826A (Leu276Ileu) mutation, including five that were homozygous for this change. Linkage analysis identified at least two possible haplotypes in linkage disequilibrium with this mutation. Patients with the C826A change had the clinically less severe LGMD2I phenotype, suggesting that this is a less disruptive FKRP mutation than those found in MDC1C. The spectrum of LGMD2I phenotypes ranged from infants with an early presentation and a Duchenne-like disease course including cardiomyopathy, to milder phenotypes compatible with a favourable long-term outcome.

Item Type:Article
Additional Information:
Keywords:Laminin alpha-2-chain gene, Merosin deficiency, Fukuyama-type, Dystroglycan, Family.
Full text:Full text not available from this repository.
Publisher Web site:http://dx.doi.org/10.1093/hmg/10.25.2851
Record Created:18 May 2007
Last Modified:08 Apr 2009 16:32

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