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59 Possible Causes for Descending Paralysis, Myasthenia Gravis, Myotonic Dystrophy

  • Progressive Bulbar Palsy

    This is the most common form of muscular dystrophy in adults Myotonic Muscular Dystrophy One thing all of these diseases have in common with an exception of Bell's Palsy is[] Clinicians frequently think of the symptoms of botulism in terms of a classic triad: bulbar palsy and descending paralysis, lack of fever, and clear senses and mental status[] Differentiation of juvenile progressive bulbar palsy from bulbar myasthenia gravis is difficult.[]

  • Accessory Nerve Palsy

    Combined III, IV, VI : stroke, tumours, Wernicke's encephalopathy, aneurysms, MS, myasthenia gravis, meningitis, muscular dystrophy, myotonic dystrophy, cavernous sinus thrombosis[] Related Articles Top 5 Articles From October 2015 An Unusual Case of Descending Paralysis Caused by West Nile Virus Clinicians should consider a diagnosis of West Nile Virus[] Examples of neuromuscular disorders include Amyotrophic lateral sclerosis Multiple sclerosis Myasthenia gravis Spinal muscular atrophy Many neuromuscular diseases are genetic[]

  • Channelopathy

    Borenstein S, Noel P, Jacquy J, Flamentdurand J (1977) Myotonic dystrophy with nerve hypertrophy.[] The genes for the construction of ion channels are highly conserved amongst mammals and one condition, hyperkalemic periodic paralysis , was first identified in the descendants[] Examples Cystic fibrosis, Dent’s disease, long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia, Brugada syndrome, myasthenia gravis,[]

  • Neuromuscular Junction Disorder

    Myasthenia gravis Myotonic dystrophy Neuromuscular junction disorders Neuromyotonia (Isaacs syndrome) Peripheral neuropathy Polymyositis Research Doctors are active in clinical[] Limb weakness may resemble that of Guillain–Barré syndrome, with ascending or descending paralysis. The reflexes are often normal.[] 2 neuromascular junction diseases 1. myasthenia gravis 2.[]

  • Congenital Slow-Channel Myasthenic Syndrome Type 4A

    […] dystophy type 1 myotonic dystrophy ( 25% of infants born to mothers with myotonic dystrophy) hypotonia and weakness of the face and limbs in infancy global developmental[] In contrast to the typical patient with GBS, botulism is sometimes said to produce an acute “descending paralysis.”[] However CMS is often included in the breadth of work of organizations whose focus is myasthenia gravis, including: Myasthenia Gravis Foundation of America (MGFA) Myasthenia[]

  • Neuromuscular Junction Disease

    Pathohistological changes in endomyocardial biopsy specimens in patients with myotonic dystrophy. Panminerva Med 1999;41:27–30. 5.[] Autonomic dysfunction (blurred vision, diplopia, bradycardia, and hypotension) followed by descending flaccid paralysis occur Wound botulism Results from contamination of[] (reference 5) Here is a list of the diseases: Myasthenia Gravis, Neonatal Myasthenia Gravis, Drug Induced Myasthenia Gravis and several types of Congenital myasthenia where[]

  • Slow-Channel Congenital Myasthenic Syndrome

    , congenital myotonic dystrophy , mitochondrial myopathy, Möbius syndrome, congenital fibrosis of EOM, infantile botulism Children and adults Mitochondrial myopathy, motor[] In contrast to the typical patient with GBS, botulism is sometimes said to produce an acute “descending paralysis.”[] […] and varied needs of patients with myasthenia gravis.[]

  • Adult Primary Lateral Sclerosis

    Strength training in patients with myotonic dystrophy and hereditary motor and sensory neuropathy: a randomized clinical trial.[] References Mills CK: Unilateral ascending paralysis and unilateral descending paralysis. JAMA 1906;47:1638-1645.[] gravis Myositis Mitochondrial myopathies Metabolic myopathies Muscular dystrophy Myotonia Isaac's syndrome Interventions Interventions offered by the Neuromuscular Disorders[]

  • Normokalemic Periodic Paralysis

    Three genetically different groups of myotonic disease can be discerned: (1) the chloride channel myotonias, (2) the adynamiaparamyotonia complex, and (3) myotonic dystrophy[] We identified the Met1592Val mutation of SCN4A in an affected descendent of this original normoKPP family.[] Because of this progress, we are now recognizing new neuromuscular di seases as well as diagnosing more subtle cases of myasthenia gravis, myotonia, and metabolic myopathies[]

  • Chest Wall Disorder

    (e.g., Duchenne dystrophy, myotonic dystrophy) Treatment Sleeping in an upright position or nocturnal use of a thoracoabdominal cuirass negative-pressure device can facilitate[] […] such as Duchenne, Becker, and limb-girdle Myasthenia gravis Myopathies (congenital, metabolic, and polymyositis) Myotonic dystrophy Post-polio syndrome Spinal cord injury[] Ventilatory support in congenital neuromuscular disorders: congenital myopathies, congenital muscular dystrophies, congenital myotonic dystrophy amd SMA II.[]

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