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5,139 Possible Causes for Electromyogram Abnormal, Hyperactive Brainstem Reflexes, Rapid Progression

  • Progressive Muscular Atrophy

    Rapid progression and typical ubiquitinated inclusions in lower motor neurons were present in 77 (95%) of the cases.[] […] tendon reflexes, and Babinski signs.[] Kovacs, Sandor Czirjak, Peter Pusztai, Ibolya Varga and Karoly Racz, Rapid Progression of Amyotrophic Lateral Sclerosis in an Acromegalic Patient After Surgical Resection[]

  • Progressive Bulbar Palsy

    A 12-month-old boy with progressive cranial nerve palsies followed by ventilatory failure demanding artificial ventilation, generalized muscle weakness, and rapid progression[] Pseudobulbar palsy is a clinical syndrome of dysarthria, dysphagia, a hyperactive gag reflex and labile emotional responses.[] Usually the onset is gradual but younger patients may show a more rapid progression.[]

  • Motor Neuron Disease

    […] tendon reflexes, and Babinski signs.[] Both cases showed rapid progression to mutism within a few years. Neuropathologically, frontal lobe degeneration including the precentral gyrus was observed.[] Usually the onset is gradual but younger patients may show a more rapid progression.[]

  • Peripheral Neuropathy

    Peripheral neuropathy may be acute (with sudden onset, rapid progress) or chronic (symptoms begin subtly and progress slowly), and may be reversible or permanent.[] Rapid communication between the peripheral nervous system and the central nervous system often depends on myelination, a process through which special cells called Schwann[] INC is also developing and testing biomarkers (signs that can indicate the diagnosis or progression of a disease) and clinical outcome measures that will be needed in future[]

    Missing: Hyperactive Brainstem Reflexes
  • Becker Muscular Dystrophy

    […] changes in the structure of the muscle cells Tests that stain the muscle sample can be used to visualize any muscle proteins present Electromyogram (EMG): Another diagnostic[] The rapid progress of research on the structure of the dystrophin gene has enormously increased our understanding of the molecular basis of Duchenne (DMD) and Becker (BMD)[] progression of both conditions.[]

    Missing: Hyperactive Brainstem Reflexes
  • Muscular Dystrophy

    This type usually occurs in the first to third decades of life and involves: the proximal (back of the body) muscles of the pelvis and shoulders slow to fairly rapid progressive[] The most common type of muscular dystrophy causes rapid muscle wasting and progressive weakness early in life, usually between the ages of 2 and 5.[] It progresses slowly, with short periods of rapid muscle deterioration and weakness. Severity ranges from very mild to completely disabling.[]

    Missing: Hyperactive Brainstem Reflexes
  • Overlap Syndrome

    Diffuse disease can involve skin hardness and thickening along the whole length of the arms and legs, face, and torso, with rapid progression.[] A 38-year-old African-American woman with an unusually rapid progression of “Primary Biliary Cirrhosis”: a missed opportunity! Semin Liver Dis 2002; 22 :395–406.[] A 38-year -old African American woman with an unusually rapid progression of "Primary Biliary Cirrhosis": A missed opportunity! Semin Liver Dis 2002;22:395-406. 52.[]

    Missing: Hyperactive Brainstem Reflexes
  • Duchenne Muscular Dystrophy

    Duchenne muscular dystrophy is a severe recessive X-linked form of muscular dystrophy characterized by rapid progression of muscle degeneration.[] It is characterized by rapid progression of muscle degeneration, eventually leading to loss of skeletal muscle control, respiratory failure, and death.[] Olson also said that progress would be rapid. “To launch a clinical trial, we need to scale up, improve efficiency and assess safety,” Dr. Olson said.[]

    Missing: Hyperactive Brainstem Reflexes
  • Amyotrophic Lateral Sclerosis

    We herein report a 15-year-old girl who developed rapid progressive muscle weakness soon after the third injection of a bivalent human papilloma virus (HPV) vaccine.[] Amyotrophic lateral sclerosis (ALS) differs from other neurodegenerations by its rapid progression and impairment of motor, cognitive, and behavioural function, which contribute[]

    Missing: Hyperactive Brainstem Reflexes
  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    […] tendon reflexes, and Babinski signs.[] Disease progression was rapid, and the majority of patients died from respiratory failure within 1–5 years after onset of disease.[] Hereditary pure lower motor neuron disease with adult onset and rapid progression. J Neurol 2001 ; 248 : 290 –96.[]

    Missing: Electromyogram Abnormal

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