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238 Possible Causes for Amyotrophic Lateral Sclerosis, Myoclonic Jerking

  • Dementia

    KEYWORDS: Amyotrophic lateral sclerosis; Positron emission tomography; Tau[] METHODS: Blood samples were collected from a family affected by ataxia, dementia, and parkinsonism, but not amyotrophic lateral sclerosis.[] […] leads to the death of neurons in amyotrophic lateral sclerosis (also known as ALS or motor neurone disease) and a common form of frontotemporal dementia.[]

  • Creutzfeldt Jakob Disease

    During the patient's hospital course, his clinical condition deteriorated with myoclonic jerks, fevers and severe encephalopathy.[] Foci of motor neuron disease in high incidence in isolated populations of East Asia and the Western Pacific. In Human Motor Neuron Diseases (ed. Rowland , L.[] Myoclonic jerks and increased muscle tone were noticed 3 months after the onset.[]

  • Amyotrophic Lateral Sclerosis

    Familial adult motor neuron disease: amyotrophic lateral sclerosis.[] Medication in the last days of life for motor neuron disease/amyotrophic lateral sclerosis . Amyotroph. Lateral Scler. 11 , 562–564 (2010). 35.[] Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial “Clinical[]

  • Alzheimer Disease

    Abstract Alzheimer disease (AD), Frontotemporal lobar degeneration (FTD), Amyotrophic lateral sclerosis (ALS) and Parkinson disease (PD) have a certain degree of clinical,[] After 36 hours of donepezil remission, the frequency of the myoclonic jerks was sharply reduced. The patient remains asymptomatic after 6 months of follow-up.[] Aluminum has been associated with neurodegenerative diseases such as Alzheimer's disease (AD), amyotrophic lateral sclerosis, and dialysis encephalopathy.[]

  • Central Nervous System Disorder

    Amyotrophic Lateral Sclerosis (ALS, Lou Gehrig's Disease) CNS Motor Disorders Etiology: Idiopathic.[] Scand J Gastroenterol 2007 ; 42 : 1088 – 94 . 9 Metals in motor neuron diseases .[] Degenerative nerve diseases include Alzheimer's disease Amyotrophic lateral sclerosis Friedreich's ataxia Huntington's disease Lewy body disease Parkinson's disease Spinal[]

  • 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[] lateral sclerosis, Frontotemporal lobar degeneration-motor neuron disease, Spinal muscular atrophy, distal SORL1 Early-onset Alzheimer disease TARDBP Amyotrophic lateral[] Overview Benign adult familial myoclonic epilepsy is an inherited epileptic syndrome characterized by cortical hand tremors , myoclonic jerks, and rare convulsive seizures[]

  • Cerebellar Disease

    jerks.[] neuron disease G12.21 Amyotrophic lateral sclerosis G12.22 Progressive bulbar palsy G12.23 Primary lateral sclerosis G12.24 Familial motor neuron disease G12.25 Progressive[] neuron disease mixed: Brown-Séquard syndrome cord syndrome ( Posterior Anterior Central / Syringomyelia ) Subacute combined degeneration of spinal cord (B12) Cauda equina[]

  • Myoclonic Jerking

    lateral sclerosis, Frontotemporal lobar degeneration-motor neuron disease, Spinal muscular atrophy, distal SORL1 Early-onset Alzheimer disease TARDBP Amyotrophic lateral[] ., adj myoclon ic. A single myoclonic arm or leg jerk is normal when the person is falling asleep. Myoclonic jerks are severe with grand mal seizures.[] These involuntary jerks are a symptom and not a disease. Myoclonic jerks are usually caused by some type of central nervous system ( brain and spinal cord ) disturbance.[]

  • Hypoparathyroidism

    INTRODUCTION: Amyotrophic lateral sclerosis (ALS) carries a grim prognosis.[]

  • Spinal Muscular Atrophy

    Here we report an adolescent female who presented with atonic and absence seizures and myoclonic jerks and was later diagnosed as having myoclonic-absence seizures.[] The latter is the only drug with proven, albeit modest, efficacy in the treatment of amyotrophic lateral sclerosis.[] neuron disease; NAA/Cr; SMA; Spinal muscular atrophy; TE; TSD; TSE; Tay–Sachs disease; amyotrophic lateral sclerosis; fluorodeoxyglucose positron emission tomography; hexosaminidase[]

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