2016
DOI: 10.1111/ene.13212
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Preferential changes of skeletal muscle echogenicity in myotonic dystrophy type 1

Abstract: Preferential high echogenicity in the medial gastrocnemius and deep finger flexors is suggestive of DM1. Muscle echogenicity is not generally related to functional dysfunction in DM1.

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Cited by 5 publications
(4 citation statements)
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“…Other muscles that are more severely affected in respective myopathies might provide more useful data. Of note, however, we have reported that gastrocnemius is one of the most severely affected muscles in IBM and DM1, (5,6) but obviously thigh and shoulder-girdle muscles should be more representative of abnormality in PM/DM.…”
Section: Study Limitationsmentioning
confidence: 77%
See 1 more Smart Citation
“…Other muscles that are more severely affected in respective myopathies might provide more useful data. Of note, however, we have reported that gastrocnemius is one of the most severely affected muscles in IBM and DM1, (5,6) but obviously thigh and shoulder-girdle muscles should be more representative of abnormality in PM/DM.…”
Section: Study Limitationsmentioning
confidence: 77%
“…As previously reported, IBM and DM1 showed preferential high echodensity regions in the medial gastrocnemius. (5,6) The representative view of LifeX texture analytic system is shown in Figure 2. Based on the calculated texture features as shown in the superimposed spreadsheet, the following analyses were performed.…”
Section: Sonographymentioning
confidence: 99%
“…Hierdurch sind einzelne Muskeln sowie tiefer liegende Knochenstrukturen teilweise gar nicht mehr abgrenzbar. Ähnliche Veränderungen wurden auch bei Patienten mit myotoner Dystrophie Typ I und II berichtet [46,47]. Diese Echogenitätsveränderungen können bei Muskeldystrophien als Verlaufsparameter verwendet werden, da gezeigt wurde, dass sie mit dem klinischen Verlauf korrelieren [48].…”
Section: Muskeldystrophienunclassified
“…Neuromuscular disorders encompassing primary myopathies, neuropathies and diseases of the neuromuscular junction are together a group of diseases that are often challenging to disentangle diagnostically . Many of these have a genetic basis and novel causative mutations continue to be identified and the clinical phenotype of existing mutations more clearly defined .…”
mentioning
confidence: 99%