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87 Possible Causes for Involuntary Movements, Myoclonic Jerking, Progressive Liver Disease

  • Wilson Disease

    jerking similar to that seen in progressive myoclonic syndrome.[web.archive.org] movements, spastic contractures, psychic disturbances, and progressive weakness and emaciation.[whonamedit.com] Editorial Editorial More on this topic Progressive lenticular degeneration: a familial nervous disease associated with cirrhosis of the liver, by S. A.[doi.org]

  • Epilepsia Partialis Continua

    Abstract We used electroencephalographic (EEG) dipole analysis to investigate the generators of spikes with and without myoclonic jerks in a 12-year-old patient with epilepsia[ncbi.nlm.nih.gov] We describe a young patient affected by schizencephaly and continuous involuntary movements of the contralateral hand.[ncbi.nlm.nih.gov] Progressive cerebral degeneration of childhood with liver disease (Alpers Huttenlocher disease) with cytochrome oxidase deficiency presenting with epilepsia partialis continua[scielo.br]

  • Levodopa

    movements, leading to progressive disability.[ncbi.nlm.nih.gov] After 4 months of remission, the disease progressed.[doi.org] Involuntary movements (dyskinesia) With long-term use of levodopa you may experience involuntary movements (dyskinesia).[parkinsons.org.uk]

  • Myoclonic Dystonia Type 15

    Usually dystonia is the prominent symptom and the myoclonic jerk involves the same body region; this condition, currently defined as " myoclonic dystonia," is included in[moh-it.pure.elsevier.com] Involuntary movements compose a group of uncontrolled movements that may manifest as a tremor, tic, myoclonic jerk, chorea, athetosis, dystonia or hemiballism.[stanfordmedicine25.stanford.edu] Metabolic tests may include screening for treatable disorders such as Wilson's disease.[endoflifecare.tripod.com]

  • Familial Progressive Myoclonic Epilepsy

    jerks may occur as a component of an absence seizure or at the onset of a GTCS Early Infantile Myoclonic Encephalopathy (Otohara Syndrome) General features: Initial seizures[neurodiffdx.com] This volume focuses on Parkinsonism and dyskinesia, a condition characterized by abnormal involuntary movements.[books.google.de] Infantile Poliodystrophy Alpers Syndrome Alpers-Huttenlocher Syndrome Neuronal Degeneration Of Childhood With Liver Disease, Progressive MTDPS4A PNDC 203700 Genetic Test[ukgtn.nhs.uk]

  • Familial Cortical Myoclonus

    Physiological: Jerks associated with sleep  occur during sleep or sleep transitions  Partial myoclonic jerks – multifocal, s/i distal muscles  Massive myoclonic jerks[slideshare.net] OBJECTIVE: Myoclonus is characterized by sudden, brief involuntary movements, and its presence is debilitating.[ncbi.nlm.nih.gov] Metabolic tests may include screening for treatable disorders such as Wilson's disease.[endoflifecare.tripod.com]

  • Central Nervous System Disorder

    There were significantly more signs of central nervous system dysfunction in the OCD group, as shown by abnormalities in fine motor coordination, involuntary and mirror movements[ncbi.nlm.nih.gov] TABLE 1 Neurological diseases involving copper metabolism Disease Characteristics Neuronal effects Aceruloplasminemia Autosomal recessive trait Progressive neurodegeneration[ajcn.nutrition.org] movements that involve several parts of the body (head, limbs, trunk, respiratory muscles); b) dysphasic dyskinesia, namely involuntary movements (choreoathetosic) that manifest[zambonpharma.com]

  • Senile Chorea

    Physiologic myoclonus is often normal in people, for example myoclonic jerks during sleep transitions.[stanfordmedicine25.stanford.edu] ., ceruloplasmin , liver enzymes ) Abdominal imaging ( hepatomegaly and/or splenomegaly ) Liver biopsy (if other diagnostics are inconclusive) Creutzfeldt-Jakob disease Very[amboss.com] […] abscess Quality and safety Rabies Radial head subluxation Radial neuropathies Rapidly progressive glomerulonephritis Rare inherited syndromes Rare neurological diseases Rare[amboss.com]

  • Neuronal Ceroid Lipofuscinosis

    jerk and visual impairment.[ncbi.nlm.nih.gov] […] of involuntary movements in JNCL, and even less do we know concerning their etiology.[dovepress.com] Progressive increases in the plasma activity levels of alanine aminotransferase and creatine kinase indicated development of pathology in the liver and muscles.[ncbi.nlm.nih.gov]

  • Primary Torsion Dystonia

    […] movements( often myoclonic jerks) and progression of symptoms leading to sustained or fixed postures.[dystonia.ie] Indeed, abnormal basal ganglia opioid transmission has been reported in several involuntary movement disorders, including levodopa-induced dyskinesias in Parkinson's disease[ncbi.nlm.nih.gov] Huntington’s Disease, also known as Huntington’s chorea is a hereditary progressive neurodegenerative disorder that results in behavioral and psychiatric abnormalities, cognitive[dystonia-parkinson.org]

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