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Results 1 - 10 of 93 for Palsy
  1. Hyperkalemic periodic paralysis 
    Hyperkalemic periodic paralysis is a condition that causes episodes of extreme muscle weakness or paralysis, usually beginning in infancy or early childhood. Most ...
    https://medlineplus.gov/.../hyperkalemic-periodic-paralysis - Genetics
  2. Horizontal gaze palsy with progressive scoliosis 
    Horizontal gaze palsy with progressive scoliosis (HGPPS) is a disorder that affects vision and also causes an abnormal curvature of the spine (scoliosis). People ...
    https://medlineplus.gov/...tal-gaze-palsy-with-progressive-scoliosis - Genetics
  3. Progressive supranuclear palsy 
    Progressive supranuclear palsy is a brain disorder that affects movement, vision, speech, and thinking ability (cognition). The signs and symptoms of this disorder ...
    https://medlineplus.gov/.../condition/progressive-supranuclear-palsy - Genetics
  4. Hereditary neuropathy with liability to pressure palsies 
    Hereditary neuropathy with liability to pressure palsies is a disorder that affects peripheral nerves. These nerves connect the brain and spinal cord to muscles ...
    https://medlineplus.gov/...opathy-with-liability-to-pressure-palsies - Genetics
  5. Hypokalemic periodic paralysis 
    Hypokalemic periodic paralysis is a condition that causes episodes of extreme muscle weakness typically beginning in childhood or adolescence. Most often, ... arms and legs. Attacks cause severe weakness or paralysis that usually lasts from hours to days. Some ...
    https://medlineplus.gov/.../condition/hypokalemic-periodic-paralysis - Genetics
  6. Infantile-onset ascending hereditary spastic paralysis 
    Infantile-onset ascending hereditary spastic paralysis is one of a group of genetic disorders known as hereditary spastic paraplegias. These disorders are characterized by progressive muscle stiffness ( ...
    https://medlineplus.gov/...et-ascending-hereditary-spastic-paralysis - Genetics
  7. Andersen-Tawil syndrome 
    ... disorder that causes episodes of muscle weakness (periodic paralysis), changes in heart rhythm (arrhythmia), and developmental abnormalities. Periodic paralysis begins early in life, and episodes last from ...
    https://medlineplus.gov/genetics/condition/andersen-tawil-syndrome - Genetics
  8. Riboflavin transporter deficiency neuronopathy 
    ... the pontobulbar region. Damage to these nerves causes paralysis of the muscles controlled by them, a condition called pontobulbar palsy. Nerves in the pontobulbar region help control several ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  9. Paramyotonia congenita 
    ... has one parent with the condition. Eulenburg disease Paralysis periodica paramyotonia Paramyotonia congenita of von Eulenburg PMC ... muscle weakness on quality of life in periodic paralysis: a survey of 66 patients. Acta Myol. 2012 ...
    https://medlineplus.gov/genetics/condition/paramyotonia-congenita - Genetics
  10. Horner syndrome 
    ... one side of the face and results from paralysis of certain nerves. Horner syndrome can appear at ... identified. Bernard-Horner syndrome Horner's syndrome Oculosympathetic palsy Von Passow syndrome Congenital Horner syndrome National Organization ...
    https://medlineplus.gov/genetics/condition/horner-syndrome - Genetics
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