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• W2391753705 abstract "Introduction Myoclonus Dystonia (M-D) is a young onset movement disorder typically involving myoclonus and dystonia of the upper body. A proportion of cases are caused by mutations to the autosomal dominantly inherited, maternally imprinted, epsilon-sarcoglycan gene (SGCE). Despite several sets of diagnostic criteria, identification of patients most likely to have an SGCE mutation remains difficult. Methods Forty consecutive patients meeting pre-existing diagnostic clinical criteria for M-D underwent a standardised clinical examination (20 SGCE-mutation positive and 20 negative). Each video was reviewed and systematically scored by two assessors blinded to mutation status. In addition, the presence and co-existence of myoclonus and dystonia was recorded in four body regions (neck, arms, legs and trunk) at rest and with action. Results Thirty-nine patients were included in the study (one case was excluded owing to insufficient video footage). Based on previously proposed diagnostic criteria patients were subdivided into 24 ‘definite’, 5 ‘probable’ and 10 ‘possible’ M-D. Motor symptom severity was higher in the SGCE mutation negative group. Myoclonus and dystonia were most commonly observed in the neck and upper limbs of both groups. Truncal dystonia with action was significantly more seen in the mutation negative group (p < 0.05). Co-existence of myoclonus and dystonia in the same body part with action was more commonly seen in the mutation negative cohort (p < 0.05). Conclusion Truncal action dystonia and co-existence of myoclonus and dystonia in the same body part with action might suggest the presence of an alternative mutation in patients with M-D." @default.
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• W2391753705 date "2016-05-13" @default.
• W2391753705 modified "2023-10-11" @default.
• W2391753705 title "Distribution and Coexistence of Myoclonus and Dystonia as Clinical Predictors of SGCE Mutation Status: A Pilot Study" @default.
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• W2391753705 doi "https://doi.org/10.3389/fneur.2016.00072" @default.
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