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328 Possible Causes for Generalized Dystonia, Myalgia, Myopathy

  • Rhabdomyolysis

    (2) Crush Injury and Trauma In crush injury and other forms of trauma, rhabdomyolysis is generally due to direct muscle injury and ischaemia.[] , myalgia and cramps, creatine kinase elevation, no weakness and often muscle hypertrophy. 2017 John Wiley & Sons A/S.[] […] for patients with mitochondrial myopathies. 5 Conclusion Mitochondrial myopathies should be considered in patients presenting with recurrent muscle pain and elevation of[]

  • Stiff-Person Syndrome

    Initial misdiagnoses included functional movement disorder (n   2), generalized dystonia and parkinsonism (n   1), and hereditary spastic paraparesis (n   1).[] […] disorders of muscle 2016 2017 2018 2019 Non-Billable/Non-Specific Code Type 1 Excludes alcoholic myopathy ( G72.1 ) cramp and spasm ( R25.2 ) drug-induced myopathy ( G72.0 ) myalgia[] Prior diagnoses included psychogenic movement disorder (n   2), idiopathic generalized dystonia and parkinsonism (n   1), and hereditary spastic paraparesis (n   1).[]

  • Myoglobinuria

    We studied an 8-year-old boy of non-Jewish, Mexican-American descent with autosomal-dominant dystonia musculorum deformans who developed rapidly progressive and severe generalized[] Each patient reported exertional myalgia, and had had at least two episodes of myoglobinuria following exertion or infection.[] We report on a 23-year-old man in whom recurrent myoglobinuria was observed due to necrotizing vacuolar myopathy confirmed on muscle biopsy.[]

  • Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency

    Generalized GALE-D Generalized GALE deficiency Generalized hematopoietic hypoplasia Generalized isolated dystonia Generalized junctional epidermolysis bullosa, non-Herlitz[] […] deficiency Disease definition Muscle beta-enolase deficiency is a glycolysis disorder reported in one patient to date and characterized clinically by exercise intolerance and myalgia[] Elsevier Health Sciences, ٢٣‏/٠٧‏/٢٠١٤ - 14 من الصفحات Congential myopathies, Muscular dystropies, Glycogen storage diseases of muscle, and Idiopathic and Inflammatory myopathies[]

  • Genetic Recurrent Myoglobinuria

    Severe dystonia and myoglobinuria. Neurology 32 : 1195 – 1197. Jardon, O.M. ( 1982 ). Physiologic stress, heat stroke, malignant hyperthermia—a perspective.[] We describe a 39-year-old woman with myalgia and exercise-related recurrent myoglobinuria, who harbored a novel mitochondrial DNA mutation at nucleotide 4281 (m.4281A G) in[] Mitochondrial Myopathies Mitochondrial myopathies are emerging as a more frequent cause of metabolic myopathy than previously recognized.[]

  • Autosomal Dominant Myoglobinuria

    Cognitive impairment Ataxia Generalized hypotonia Intellectual disability Distal upper limb amyotrophy Mild proteinuria Distal lower limb amyotrophy Axonal loss Onion bulb[] Suite gene sharing: Human phenotypes related to Myoglobinuria, Autosomal Dominant: 33 # Description HPO Frequency HPO Source Accession 1 muscle weakness 33 HP:0001324 2 myalgia[] Elsevier Health Sciences, ٢٣‏/٠٧‏/٢٠١٤ - 14 من الصفحات Congential myopathies, Muscular dystropies, Glycogen storage diseases of muscle, and Idiopathic and Inflammatory myopathies[]

  • Idiopathic Camptocormia

    […] was a case of generalized dystonia with camptocormia.[] Marked myalgia was commonly associated. Serum creatine kinase levels were normal or moderately elevated.[] The cause of camptocormia in idiopathic PD is a focal myopathy.[]

  • Autosomal Dominant Progressive External Ophthalmoplegia Type 6

    In addition to LHON this mutation also presents with generalized dystonia associated with bilateral striatal necrosis (LDYT).[] Autosomal Dominant 6, is also known as progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6, and has symptoms including muscle cramp, myalgia[] Acquired myopathies can be subclassified as inflammatory myopathies, toxic myopathies, and myopathies associated with systemic conditions.[]

  • Influenza

    Previously described patients have suffered from acute-onset myoclonus and/or dystonia or post-viral parkinsonism.[] It is marked by inflammation of the nasal mucosa; the pharynx; and conjunctiva, and by headache and severe, often generalized, myalgia.[] Immune-mediated necrotizing myopathy is a very rare inflammatory disease affecting skeletal muscles.[]

  • Fibromyalgia

    The generalized dystonia was probably due to the patient's analgesic protective attitude. The actual therapy is still based on the biopsychosocial approach.[] Myalgia and arthralgia was observed in chronic EMS in the same incidence as in patients with FMS (81%).[] Myopathy with Lactic Acidosis, Hereditary Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset Myopathy, Granulovacuolar Lobular, with Electrical Myotonia[]

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