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Lookup NU author(s): Dr Daniel Birchall, Professor Volker StraubORCiD, Professor Hanns Lochmuller, Professor Patrick Chinnery
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Distal myopathies are a clinically and genetically heterogenous group of disorders in which the distal limb musculature is selectively or disproportionately affected. Precisely defining specific categories is a challenge because of overlapping clinical phenotypes, making it difficult to decide which of the many known causative genes to screen in individual cases. In this study we define the distinguishing magnetic resonance imaging findings in myotilin myopathy by studying 8 genealogically unrelated cases due to the same point mutation in TTID. Proximally, the vastii, biceps femoris and semimembranosus were involved with sparing of gracilis and sartorius. Distally, soleus, gastrocnemius, tibialis anterior, extensor hallicus and extensor digitorum were involved. This pattern contrasts with other distal myopathies and provides further support for the role of imaging in the clinical investigation of muscle disease. Copyright (C) 2009 S. Karger AG, Basel
Author(s): McNeill A, Birchall D, Straub V, Goldfarb L, Reilich P, Walter MC, Schramm N, Lochmuller H, Chinnery PF
Publication type: Article
Publication status: Published
Journal: European Neurology
Year: 2009
Volume: 62
Issue: 3
Pages: 161-166
Print publication date: 01/01/2009
ISSN (print): 0014-3022
ISSN (electronic):
Publisher: S. Karger AG
URL: http://dx.doi.org/10.1159/000227266
DOI: 10.1159/000227266
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