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549 Possible Causes for Dehydration, Generalized Dystonia, Myopathy

  • Rhabdomyolysis

    At presentation, she was dehydrated. Blood analysis revealed acute renal failure and increased muscular enzymes.[] (2) Crush Injury and Trauma In crush injury and other forms of trauma, rhabdomyolysis is generally due to direct muscle injury and ischaemia.[] […] for patients with mitochondrial myopathies. 5 Conclusion Mitochondrial myopathies should be considered in patients presenting with recurrent muscle pain and elevation of[]

  • Muscle Spasm

    Disclaimer The Dystonia Society provides the information on this page as general information only.[] Cause of Exercise Associated Muscle Cramps (EAMC) — altered neuromuscular control, dehydration or electrolyte depletion?[] .- ) muscular dystrophies and myopathies ( G71 - G72 ) myopathy in amyloidosis ( E85.- ) myopathy in polyarteritis nodosa ( M30.0 ) myopathy in rheumatoid arthritis ( M05.32[]

  • Muscle Cramp

    Neuromuscular control may be more important in the onset of muscle cramps than dehydration or electrolyte losses.[] ., any involuntary and abnormal muscle contraction, regardless of whether it is painful) or generic painful contractions based on clinical and electrophysiological criteria[] Muscular system: Some myopathies (diseases that affect skeletal muscles); and Myotonia (temporary muscle stiffness or contraction).[]

  • Glutaric Aciduria

    It presents early in life, usually after an episode of fever, dehydration, infection or fasting, and results in metabolic decompensation and neurologic damage.[] Initiation of treatment after the onset of symptoms is generally less effective. Secondary dystonia is often difficult to treat.[] KEYWORDS: glutaric aciduria type II; multiple acyl Co-A dehydrogenase deficiency; myopathy; rhabdomyolysis[]

  • Adult-Onset Cervical Dystonia Type DYT23

    [Raoul] HENNEKAM Dr A.Micheil INNES Pr Harald JÜPPNER Dr Agnieszka JURECKA Pr Jean KANITAKIS Pr Alexander KATOULIS Disease name Simpson-Golabi-Behmel syndrome Dehydrated hereditary[] DYT1 dystonia typically presents as early onset, generalized dystonia, starting in the legs.[] COL6A1 Bethlem myopathy COL6A2 Bethlem myopathy type 1 COL6A3 Bethlem myopathy type 2 COL12A1 Borjeson-Forssman-Lehmann syndrome PHF6 Brody myopathy ATP2A1 Brunner syndrome[]

  • Hereditary Cryohydrocytosis with Reduced Stomatin

    […] epilepsy with febrile seizures plus 3 AD 15 JRK 603210 22 SLC2A1 138140 Dystonia-9; GLUT1 deficiency syndrome; dystonia 18; Epilepsy, idiopathic generalized, suscpetibility[] Dehydrated with perinatal ascites It was Entazami and others (1997) who first noted a link between dehydrated HSt and a syndrome of 'perinatal ascites' (ie accumulation of[] Myopathy, centronuclear NEB Nemaline myopathy TNNT1 Nemaline myopathy TPM2 Arthrogryposis, distal, CAP myopathy, Nemaline myopathy TPM3 CAP myopathy, Myopathy, congenital[]

  • Myoglobinuria

    In a runner, myoglobinuria can be caused by severe, prolonged muscle stress (as in a marathon) combined with heat and dehydration.[] 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[] We report on a 23-year-old man in whom recurrent myoglobinuria was observed due to necrotizing vacuolar myopathy confirmed on muscle biopsy.[]

  • Alzheimer Disease

    Death certificates of AD subjects were more likely to list dementia/AD, other brain disorders, pneumonia, and dehydration, and less likely to include cancer.[] A four-generation pedigree exhibiting early-onset autosomal dominant Alzheimer disease (AD) with spastic paraplegia, dystonia, and dysarthria due to a novel 6-nucleotide insertional[] […] account for the myopathy has also been suggested [ 44 ].[]

  • Amyotrophic Lateral Sclerosis Type 5

    And the other thing is the deterioration of swallowing muscles, and that can lead to malnutrition and dehydration.[] ALS2 mutations: Juvenile amyotrophic lateral sclerosis and generalized dystonia.[] […] dementia, BSCL2 -related neurologic disorders, DCTN1 -related distal hereditary motor neuronopathy type VIIB, GBE1 -related adult polyglucosan body disease, and inclusion body myopathy[]

  • Methylmalonic Acidemia

    She had clinical signs of diabetic ketoacidosis such as dehydration, deep sighing respiration, smell of ketones, lethargy, and vomiting.[] A 14 month-old boy presented with an acute generalized dystonia and lethargy preceded by fever, vomiting and lethargy at the age of 13 months.[] The myopathy may not be reversible despite treatment, leading to continued gait disturbances.[]

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