Publication:
Myotonic Dystrophy

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dc.contributor.authorApostolski, Slobodan (7004532054)
dc.contributor.authorRakocevic-Stojanovic, Vidosava (6603893359)
dc.date.accessioned2025-06-12T23:02:42Z
dc.date.available2025-06-12T23:02:42Z
dc.date.issued2010
dc.description.abstract[No abstract available]
dc.identifier.urihttps://doi.org/10.1002/9781444317008.ch61
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84885506711&doi=10.1002%2f9781444317008.ch61&partnerID=40&md5=29ac6accfe8fdce0d9a46285e7588b8c
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/10263
dc.subjectAtrophy and weakness of sternomastoids and hyperlordosis of neck ("swan neck")
dc.subjectElectromyogram (EMG) investigation - revealing electrical myotonia
dc.subjectGastrointestinal symptoms - in as many as 80% of patients
dc.subjectIridiscent posterior subcapsular cataracts (metachromatic or "Christmas tree") - found by slit-lamp examination
dc.subjectMyotonic dystrophy (DM, dystrophia myotonica or Steinert's disease) - most common form of muscular dystrophy in adults
dc.subjectMyotonic dystrophy type 1 (DM1)
dc.subjectMyotonic dystrophy type 1 (DM1), by aberrantly expanded CTG repeat in 3′-untranslated region of DM protein kinase (DMPK) gene
dc.subjectMyotonic dystrophy type 2 (DM2)
dc.subjectPrevalence of DM1 - approximately 5 per 100 000 in American and European populations
dc.titleMyotonic Dystrophy
dspace.entity.typePublication

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