Magnetic resonance imaging pattern variability in dysferlinopathy

التفاصيل البيبلوغرافية
العنوان: Magnetic resonance imaging pattern variability in dysferlinopathy
المؤلفون: Sergey N, Bardakov, Vadim A, Tsargush, Pierre G, Carlier, Sergey S, Nikitin, Sergey A, Kurbatov, Angelina A, Titova, Zoya R, Umakhanova, Patimat G, Akhmedova, Raisat M, Magomedova, Igor S, Zheleznyak, Alexander A, Emelyantsev, Ekaterina N, Berezhnaya, Ivan, A Yakovlev, Artur A, Isaev, Roman V, Deev
المصدر: Acta Myologica
سنة النشر: 2021
مصطلحات موضوعية: Muscular Diseases, Muscular Dystrophies, Limb-Girdle, MRI pattern, Miyoshi myopathy, Humans, Original Article, T2-MSME, Muscle, Skeletal, Magnetic Resonance Imaging, dysferlinopathy, LGMDR2, LGMD2B
الوصف: The widespread use of magnetic resonance imaging (MRI) in the diagnosis of myopathies has made it possible to clarify the typical MRI pattern of dysferlinopathy. However, sufficient attention has not been given to the variability of MRI patterns in dysferlinopathy. Materials and methods Twenty-five patients with the clinical manifestations of dysferlinopathy were examined. For all patients, creatine phosphokinase levels were measured and molecular genetics were examined. In two patients, immunohistochemical examinations of muscle biopsies were performed. MRI scanning was included T2 multi-slice multi-echo, T1 weighted, T2 weighted and Short Tau Inversion Recovery T2 weighted sequences. Quantitative and semi-quantitative evaluations of fatty replacement and swelling of the muscles were undertaken. Results Variability in the MRI patterns was lowest in the pelvis and leg muscles and highest in the thigh muscles. Three main types of MRI patterns were distinguished: posterior-dominant (80%), anterior-dominant (16%), and diffuse (4%). Among patients with the anterior-dominant pattern, the collagen-like variant (4%), proximal variant (4%) and pseudo-myositis (8%) were separately distinguished. Conclusions Awareness of atypical MRI patterns in dysferlinopathy is important for increasing the efficiency of routine diagnostics and optimizing the search for causative gene mutations.
تدمد: 2532-1900
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::cac65c3e0baec8f89ba370b49b293eef
https://pubmed.ncbi.nlm.nih.gov/35047756
حقوق: OPEN
رقم الأكسشن: edsair.pmid..........cac65c3e0baec8f89ba370b49b293eef
قاعدة البيانات: OpenAIRE