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Results 1 - 10 of 73 for cerebral palsy
  1. Dopamine transporter deficiency syndrome 
    ... underdiagnosed because its signs and symptoms overlap with cerebral palsy and other movement disorders. Dopamine transporter deficiency syndrome is caused by mutations in the SLC6A3 gene. This gene provides instructions for ... in the brain, where it transports a molecule called dopamine into ...
    https://medlineplus.gov/.../dopamine-transporter-deficiency-syndrome - Genetics
  2. ADCY5-related dyskinesia 
    ... can resemble those of other conditions such as cerebral palsy or epilepsy. As its name suggests, ADCY5-related ...
    https://medlineplus.gov/genetics/condition/adcy5-related-dyskinesia - 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 usually ...
    https://medlineplus.gov/.../condition/progressive-supranuclear-palsy - Genetics
  4. Farber lipogranulomatosis 
    ... fluid in the brain (hydrocephalus), loss (atrophy) of brain tissue, paralysis of the arms and legs (quadriplegia), loss of ...
    https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis - Genetics
  5. 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
  6. Transthyretin amyloidosis 
    ... the brain, an accumulation of fluid in the brain (hydrocephalus), difficulty coordinating movements (ataxia), muscle stiffness and weakness (spastic paralysis), seizures, and loss of intellectual function (dementia). Eye ...
    https://medlineplus.gov/genetics/condition/transthyretin-amyloidosis - Genetics
  7. Hyperkalemic periodic paralysis 
    ... 129(Pt 1):8-17. doi: 10.1093/brain/awh639. Epub 2005 Sep 29. Citation on PubMed Weber F. Hyperkalemic Periodic Paralysis. 2003 Jul 18 [updated 2021 Jul 1]. In: ...
    https://medlineplus.gov/.../hyperkalemic-periodic-paralysis - Genetics
  8. Cerebral cavernous malformation 
    ... serious signs and symptoms such as headaches, seizures, paralysis, hearing or vision loss, and bleeding in the brain (cerebral hemorrhage). Severe brain hemorrhages can result in ...
    https://medlineplus.gov/.../cerebral-cavernous-malformation - Genetics
  9. Hypokalemic periodic paralysis 
    ... 129(Pt 1):8-17. doi: 10.1093/brain/awh639. Epub 2005 Sep 29. Citation on PubMed Weber F, Lehmann-Horn F. Hypokalemic Periodic Paralysis. 2002 Apr 30 [updated 2018 Jul 26]. In: ...
    https://medlineplus.gov/.../condition/hypokalemic-periodic-paralysis - Genetics
  10. 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
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