Ryanodine receptor 1 (RYR1) mutations in two patients with tubular aggregate myopathy.
Gaetano Nicola Alfio VattemiDaniela RossiLucia GalliMaria Rosaria CatalloElia PancheriGiulia MarchettoBarbara CisternaManuela MalatestaEnrico PierantozziPaola ToninVincenzo SorrentinoPublished in: The European journal of neuroscience (2022)
Two likely causative mutations in the RYR1 gene were identified in two patients with myopathy with tubular aggregates, but no evidence of cores or core-like pathology on muscle biopsy. These patients were clinically evaluated and underwent routine laboratory investigations, electrophysiologic tests, muscle biopsy and muscle magnetic resonance imaging (MRI). They reported stiffness of the muscles following sustained activity or cold exposure and had serum creatine kinase elevation. The identified RYR1 mutations (p.Thr2206Met or p.Gly2434Arg, in patient 1 and patient 2, respectively) were previously identified in individuals with malignant hyperthermia susceptibility and are reported as causative according to the European Malignant Hyperthermia Group rules. To our knowledge, these data represent the first identification of causative mutations in the RYR1 gene in patients with tubular aggregate myopathy and extend the spectrum of histological alterations caused by mutation in the RYR1 gene.
Keyphrases
- magnetic resonance imaging
- skeletal muscle
- copy number
- late onset
- genome wide
- case report
- end stage renal disease
- genome wide identification
- ultrasound guided
- newly diagnosed
- contrast enhanced
- healthcare
- computed tomography
- muscular dystrophy
- clinical practice
- fine needle aspiration
- transcription factor
- machine learning
- endothelial cells
- diffusion weighted imaging
- protein kinase
- artificial intelligence