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Tissue Triage and Freezing for Models of Skeletal Muscle Disease
Published on: July 15, 2014
Distal arthrogryposis and muscle weakness associated with a beta-tropomyosin mutation
H Tajsharghi1, E Kimber, D Holmgren
1Department of Pathology, Sahlgrenska University Hospital, SE-413 45 Göteborg, Sweden. homa.tajsharghi@pathology.gu.se
Abstract:
Tropomyosin (TM), a sarcomeric thin-filament protein, plays an essential part in muscle contraction by regulating actin-myosin interaction. We describe two patients, a woman and her daughter, with muscle weakness and distal arthrogryposis (DA) type 2B, caused by a heterozygous missense mutation, R133W, in TPM2, the gene encoding beta-TM. Our results demonstrate the involvement of muscle dysfunction in the pathogenesis of DA and the fact that DA2B may be caused by mutations in TPM2.
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