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dc.contributor.authorJensen, Synnøve
dc.contributor.authorMüller, Kai Ivar
dc.contributor.authorMellgren, Svein Ivar
dc.contributor.authorBindoff, Laurence Albert
dc.contributor.authorRasmussen, Magnhild
dc.contributor.authorØrstavik, Kristin
dc.contributor.authorJonsrud, Christoffer
dc.contributor.authorTveten, Kristian
dc.contributor.authorNilssen, Øivind
dc.contributor.authorVan Ghelue, Marijke
dc.contributor.authorArntzen, Kjell Arne
dc.date.accessioned2023-01-16T08:11:36Z
dc.date.available2023-01-16T08:11:36Z
dc.date.issued2022-11-25
dc.description.abstractWe aimed to investigate the epidemiology and natural history of FKRP-related limb-girdle muscular dystrophy R9 (LGMDR9) in Norway. We identified 153 genetically confirmed subjects making the overall prevalence 2.84/100,000, the highest reported figure worldwide. Of the 153 subjects, 134 (88 %) were homozygous for FKRP c.826C>A giving a carrier frequency for this variant of 1/101 in Norway. Clinical questionnaires and patient notes from 101 subjects, including 88 c.826C>A homozygotes, were reviewed, and 43/101 subjects examined clinically. Age of onset in c.826C>A homozygotes demonstrated a bimodal distribution. Female subjects showed an increased cumulative probability of wheelchair dependency and need for ventilatory support. Across the cohort, the need for ventilatory support preceded wheelchair dependency in one third of the cases, usually due to sleep apnea. In c.826C>A homozygotes, occurrence of cardiomyopathy correlated positively with male gender but not with age or disease stage. This study highlights novel gender differences in both loss of ambulation, need for ventilatory support and the development of cardiomyopathy. Our results confirm the need for vigilance in order to detect respiratory insufficiency and cardiac involvement, but indicate that these events affect males and females differently.en_US
dc.identifier.citationJensen, Müller, Mellgren, Bindoff, Rasmussen, Ørstavik, Jonsrud, Tveten, Nilssen, Van Ghelue, Arntzen. Epidemiology and natural history in 101 subjects with FKRP-related limb-girdle muscular dystrophy R9. The Norwegian LGMDR9 cohort study (2020). Neuromuscular Disorders. 2022en_US
dc.identifier.cristinIDFRIDAID 2095239
dc.identifier.doi10.1016/j.nmd.2022.11.005
dc.identifier.issn0960-8966
dc.identifier.issn1873-2364
dc.identifier.urihttps://hdl.handle.net/10037/28236
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.journalNeuromuscular Disorders
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.titleEpidemiology and natural history in 101 subjects with FKRP-related limb-girdle muscular dystrophy R9. The Norwegian LGMDR9 cohort study (2020)en_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution 4.0 International (CC BY 4.0)