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Results 1 - 10 of 11 for cerebral palsy
  1. MAPT gene 
    ... are essential for coordinating movement. This loss of brain cells underlies the major features of progressive supranuclear palsy, including problems with movement, vision, speech, and thinking ( ...
    https://medlineplus.gov/genetics/gene/mapt - Genetics
  2. SLC52A3 gene 
    ... Harding B, Brett EM, Wilson J. Progressive bulbar paralysis of childhood. A reappraisal of Fazio-Londe disease. Brain. 1992 Dec;115 ( Pt 6):1889-900. doi: ...
    https://medlineplus.gov/genetics/gene/slc52a3 - Genetics
  3. ROBO3 gene 
    ... in ensuring that this crossing over occurs during brain development. At least 19 different mutations in the ROBO3 gene have been identified in people with horizontal gaze palsy with progressive scoliosis (HGPPS). These mutations change the ...
    https://medlineplus.gov/genetics/gene/robo3 - Genetics
  4. ALS2 gene 
    ... 129(Pt 7):1710-9. doi: 10.1093/brain/awl104. Epub 2006 May 2. Citation on PubMed Racis L, Tessa A, Pugliatti M, Storti E, Agnetti V, Santorelli FM. Infantile-onset ascending hereditary spastic paralysis: a case report and brief literature review. Eur ...
    https://medlineplus.gov/genetics/gene/als2 - Genetics
  5. CACNA1S gene 
    ... 129(Pt 1):8-17. doi: 10.1093/brain/awh639. Epub 2005 Sep 29. Citation on ... dominant hypokalemic periodic paralysis in a Chinese family. J Mol Med (Berl). ...
    https://medlineplus.gov/genetics/gene/cacna1s - Genetics
  6. REEP1 gene 
    ... condition is characterized by muscle stiffness (spasticity) and paralysis of the lower limbs (paraplegia) caused by degeneration ... expressed in neuronal and neuronal-like exocytotic tissues. Brain Res. 2014 Jan 30;1545:12-22. doi: ...
    https://medlineplus.gov/genetics/gene/reep1 - Genetics
  7. ATP1A3 gene 
    ... condition is characterized by 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/atp1a3 - Genetics
  8. 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
  9. 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
  10. ALDH18A1 gene 
    ... by muscle stiffness (spasticity) and the development of paralysis of the lower limbs (paraplegia) caused by breakdown ... leads to dominant and recessive hereditary spastic paraplegia. Brain. 2015 Aug;138(Pt 8):2191-205. doi: ...
    https://medlineplus.gov/genetics/gene/aldh18a1 - Genetics
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