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305 Possible Causes for Generalized Dystonia, Glucose Increased, 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.[baggas.tripod.com] Using serum values, calculated osmolarity can be determined using the formula (2 x Na) (glucose/18) (BUN/2.8).[clinicaladvisor.com] […] for patients with mitochondrial myopathies. 5 Conclusion Mitochondrial myopathies should be considered in patients presenting with recurrent muscle pain and elevation of[jaoa.org]

  • Spasmodic Torticollis

    This form of focal dystonia is unlikely to spread beyond the neck and shoulders or become generalized dystonia.[dystoniacanada.org] glucose in the premotor cortex and lentiform nucleus.[symptoma.com] Such a type of focal dystonia is quite unlikely to spread outside the shoulders and neck region and become generalized dystonia.[hxbenefit.com]

  • General Anesthesia

    An 11-year-old male receiving aripiprazole, methylphenidate, and clonidine developed acute masseter dystonia inhibiting tracheal intubation after induction of general anesthesia[ncbi.nlm.nih.gov] RESULTS: Resting energy expenditure (B1: 1230 228; B2: 1317 282; C: 1012 153 kcal/h; B2 vs C, P CONCLUSIONS: The administration of amino acids and glucose increased measured[ncbi.nlm.nih.gov] […] discussing general anesthesia for adults with mitochondrial myopathy.[ncbi.nlm.nih.gov]

  • Familial Visceral Myopathy

    A missense variant (R183W) in non-muscle actin (ACTB, β-actin) has been linked to a combination of malformations, sensory hearing loss, and delayed-onset generalized dystonia[agajournals.wordpress.com] MuRF-1 was increased in accordance with muscle atrophy, MEF-2, calcineurin (CN) and GLUT-4 transporter were reduced, suggesting altered transcription, alteration of glucose[aetna.com] Histological examination of biopsy specimens and molecular analysis show that this patient had both familial visceral myopathy and a mitochondrial myopathy, suggesting that[ncbi.nlm.nih.gov]

  • Amyotrophic Lateral Sclerosis Type 5

    ALS2 mutations: Juvenile amyotrophic lateral sclerosis and generalized dystonia.[discovery.ucl.ac.uk] MRI spine has abnormal enhancement along the entire spinal cord and increased intensity in patchy areas in the conus medullaris and mid thoracic region.[kundoc.com] […] dementia, BSCL2 -related neurologic disorders, DCTN1 -related distal hereditary motor neuronopathy type VIIB, GBE1 -related adult polyglucosan body disease, and inclusion body myopathy[blueprintgenetics.com]

  • MELAS Syndrome

    ; alternating with ataxia, dystonia, choreoathetosis and spastic paraplegia.[oatext.com] We hypothesize that DM develops in individuals with MELAS syndrome due to multiple defects in glucose metabolism, including decreased glucose utilization, increased glucose[ashg.org] Abstract Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare neurodegenerative disease caused by the decreased ability[ncbi.nlm.nih.gov]

  • 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[ncbi.nlm.nih.gov] If exercise is prolonged, utilization of FFAs and blood glucose increases.[what-when-how.com] We report on a 23-year-old man in whom recurrent myoglobinuria was observed due to necrotizing vacuolar myopathy confirmed on muscle biopsy.[ncbi.nlm.nih.gov]

  • Muscle Spasm

    Disclaimer The Dystonia Society provides the information on this page as general information only.[dystonia.org.uk] Taking a warm bath before bedtime may increase circulation to the legs and reduce the incidence of nighttime leg cramps. Resources BOOKS Bradley, Walter G., et al.[encyclopedia.com] .- ) muscular dystrophies and myopathies ( G71 - G72 ) myopathy in amyloidosis ( E85.- ) myopathy in polyarteritis nodosa ( M30.0 ) myopathy in rheumatoid arthritis ( M05.32[icd10data.com]

  • Stiff-Person Syndrome

    Initial misdiagnoses included functional movement disorder (n   2), generalized dystonia and parkinsonism (n   1), and hereditary spastic paraparesis (n   1).[jamanetwork.com] Unfortunately, reintroduction of benzodiazepine was a source of rapid and high increase of CK, LDH, GADAb titer (up to 1:15,000), IGT, and SPS relapse.[ncbi.nlm.nih.gov] ( G72.1 ) cramp and spasm ( R25.2 ) drug-induced myopathy ( G72.0 ) myalgia ( M79.1- ) stiff-man syndrome ( G25.82 ) Type 2 Excludes nontraumatic hematoma of muscle ( M79.81[icd10data.com]

  • Dilated Cardiomyopathy Type 2B

    9/GLUT1 deficiency syndrome 1, infantile onset, severe/GLUT1 deficiency syndrome 2, childhood onset/Epilepsy, idiopathic generalized, susceptibility to, 12 138140 EPI Epilepsy[lhsc.on.ca] Use of some drugs, especially stimulants, may also increase blood glucose and thus increase urination.[citation needed].[en.wikipedia.org] .3,4 Furthermore myotilin mutations have now been demonstrated in myofibrillar myopathy, or desmin-related myopathy, as well as in LGMD1A.5 These observations and several[books.google.com]

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