Morten Duno
Copenhagen University Hospital
189 Papers
781 Citations
Morten Duno is an academic researcher from Copenhagen University Hospital. The author has contributed to research in topics: Medicine & Population. The author has an hindex of 35, co-authored 172 publications. Previous affiliations of Morten Duno include Aarhus University & University of Copenhagen.
Chat about Author
Papers
Delayed diagnosis of oculopharyngeal muscular dystrophy in Denmark: from initial ptosis to genetic testing
TL;DR: The first unique case of periodic esotropia with a monthly cycle and onset along with the menstrual period is presented, and it is hypothesized that underlying this strabismic condition, the patient had entire days except her menstrual period where she experienced an orthotropic burst; therefore, a trigger factor to suppress Orthotropic burst condition might also exist.
Deficiency of the α Subunit of Succinate–Coenzyme A Ligase Causes Fatal Infantile Lactic Acidosis with Mitochondrial DNA Depletion
Elsebet Ostergaard,Ernst Christensen,Elisabeth Kristensen,Bodil Mogensen,Morten Duno,Eric A. Shoubridge,Flemming Wibrand +6 more
TL;DR: A combined respiratory-chain enzyme deficiency associated with mitochondrial DNA (mtDNA) depletion in a small consanguineous family with fatal infantile lactic acidosis is found.
Novel truncating variants in FGD1 detected in two Danish families with Aarskog–Scott syndrome and myopathic features
TL;DR: Four adults with AAS from two unrelated Danish families, all males presented with variable features suggestive of myopathy, suggest that myopathic involvement should be considered in AAS.
Cardiac Involvement in Women With Pathogenic Dystrophin Gene Variants.
Tuva Åsatun Solheim,Freja Fornander,Anna Axelsson Raja,Rasmus Mogelvang,Nanna S. Poulsen,Morten Duno,Henning Bundgaard,John Vissing +7 more
TL;DR: In this article, the frequency and extent of cardiac involvement in female carriers of pathogenic variants in DMD, 53 women were examined through an observational, cross-sectional study, where they were examined by cardiac magnetic resonance imaging (CMR) with late gadolinium enhancement, echocardiography, 24-h Holter monitoring, ECG, and blood concentrations of skeletal and cardiac muscle biomarkers.
Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in Denmark.
TL;DR: Overall, genetic and histologic prevalence of congenital myopathy in Denmark differs from previous retrospective reports, and less RYR1 and more DNM2 and NEB mutations and less core histology were present in this cohort.