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Results 1 - 10 of 15 for Palsy
  1. MAPT gene 
    ... gene have been found to cause progressive supranuclear palsy. However, mutations in this gene appear to be ... with an increased risk of developing progressive supranuclear palsy. This polymorphism, known as the H1 haplotype, is ...
    https://medlineplus.gov/genetics/gene/mapt - Genetics
  2. ROBO3 gene 
    ... in people with a condition called horizontal gaze palsy with progressive scoliosis (HGPPS). At birth, individuals with ... TM. Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations. J ...
    https://medlineplus.gov/genetics/gene/robo3 - Genetics
  3. SCN4A gene 
    ... gene have been found to cause hyperkalemic periodic paralysis, a condition that causes episodes of extreme muscle ... contract, leading to episodes of muscle weakness or paralysis. More About This Health Condition At least nine ...
    https://medlineplus.gov/genetics/gene/scn4a - Genetics
  4. ALS2 gene 
    ... found to cause infantile-onset ascending hereditary spastic paralysis. This disorder is characterized by progressive weakness and ... gene mutations cause infantile-onset ascending hereditary spastic paralysis. Research suggests that a lack of alsin and ...
    https://medlineplus.gov/genetics/gene/als2 - Genetics
  5. CACNA1S gene 
    ... have been identified in people with hypokalemic periodic paralysis, a condition that causes episodes of extreme muscle ... of muscle weakness in people with hypokalemic periodic paralysis. More About This Health Condition CAC1S_HUMAN CACH1 ...
    https://medlineplus.gov/genetics/gene/cacna1s - Genetics
  6. ATP1A2 gene 
    ... of this condition is recurrent episodes of temporary paralysis, often affecting one side of the body (hemiplegia). During some episodes, the paralysis alternates from one side to the other or ...
    https://medlineplus.gov/genetics/gene/atp1a2 - Genetics
  7. PMP22 gene 
    ... cause of hereditary neuropathy with liability to pressure palsies. This disorder is characterized by recurrent episodes of ... symptoms of hereditary neuropathy with liability to pressure palsies. More About This Health Condition Having an extra ...
    https://medlineplus.gov/genetics/gene/pmp22 - Genetics
  8. ATP1A3 gene 
    ... condition is characterized by recurrent episodes of temporary paralysis that often affects only one side of the body (hemiplegia). During some episodes, the paralysis alternates from one side to the other or ...
    https://medlineplus.gov/genetics/gene/atp1a3 - Genetics
  9. SLC52A3 gene 
    ... Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54. ... Harding B, Brett EM, Wilson J. Progressive bulbar paralysis of childhood. A reappraisal of Fazio-Londe disease. ...
    https://medlineplus.gov/genetics/gene/slc52a3 - Genetics
  10. KCNJ2 gene 
    ... disorder characterized by episodes of muscle weakness (periodic paralysis), changes in heart rhythm (arrhythmia), and physical abnormalities ... ions out of these cells, resulting in periodic paralysis and an irregular heart rhythm. It is not ...
    https://medlineplus.gov/genetics/gene/kcnj2 - Genetics
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