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Bethlem Myopathy Phenotypes and Follow Up: Description of 8 Patients at the Mildest End of the Spectrum.

dc.contributor.authorCruz, S
dc.contributor.authorFigueroa-Bonaparte, S
dc.contributor.authorGallardo, E
dc.contributor.authorde Becdelièvre, A
dc.contributor.authorGartioux, C
dc.contributor.authorAllamand, V
dc.contributor.authorPiñol, P
dc.contributor.authorGarcia, MA
dc.contributor.authorJiménez-Mallebriera, C
dc.contributor.authorLlauger, J
dc.contributor.authorGonzález-Rodríguez, L
dc.contributor.authorCortes-Vicente, E
dc.contributor.authorIlla, I
dc.contributor.authorDíaz-Manera, J
dc.date.accessioned2017-06-29T10:21:09Z
dc.date.available2017-06-29T10:21:09Z
dc.date.issued2016
dc.description.abstractThe classical phenotypes of collagen VI-associated myopathies are well described. Little is known, however, about the progression of patients at the mildest end of the clinical spectrum. In this report, we describe the clinical findings and the results of MRI, muscle biopsy, collagen VI expression in cultured skin fibroblasts and genetic tests of a series of patients with Bethlem myopathy. Our series highlights the existence of mild presentations of this disorder that progresses only slightly and can easily be overlooked. Analysis of the genetic studies suggests that missense mutations can be associated to a milder clinical presentation. Muscle MRI is extremely useful as it shows a pathognomonic pattern in most patients, especially those with some degree of muscle weakness.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationJ Neuromuscul Dis. 2016 May 27;3(2):267-274.pt_PT
dc.identifier.doi10.3233/JND-150135pt_PT
dc.identifier.issn2214-3602
dc.identifier.urihttp://hdl.handle.net/10400.10/1887
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherIOS Presspt_PT
dc.subjectMuscular dystrophiespt_PT
dc.subjectBethlem diseasept_PT
dc.subjectCollagen type VIpt_PT
dc.subjectMagnetic resonance imagingpt_PT
dc.titleBethlem Myopathy Phenotypes and Follow Up: Description of 8 Patients at the Mildest End of the Spectrum.pt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceAmsterdampt_PT
oaire.citation.endPage274pt_PT
oaire.citation.startPage267pt_PT
oaire.citation.titleJournal of neuromuscular diseasespt_PT
oaire.citation.volume3pt_PT
rcaap.rightsrestrictedAccesspt_PT
rcaap.typearticlept_PT

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