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Results 1 - 10 of 10 for dyskinesia
  1. PNKD gene 
    ... have been shown to cause familial paroxysmal nonkinesigenic dyskinesia, which is characterized by episodes of involuntary movement. ... the signs and symptoms of familial paroxysmal nonkinesigenic dyskinesia. More About This Health Condition brain protein 17 ...
    https://medlineplus.gov/genetics/gene/pnkd - Genetics
  2. RPGR gene 
    ... Condition MedlinePlus Genetics provides information about Primary ciliary dyskinesia More About This Health Condition Although most RPGR ... a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa. J Med Genet. 2006 Apr; ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  3. DNAH5 gene 
    ... gene have been found to cause primary ciliary dyskinesia, which is a condition characterized by respiratory tract ... cilia lead to the features of primary ciliary dyskinesia. More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/dnah5 - Genetics
  4. PRRT2 gene 
    ... cause another neurological disorder called familial paroxysmal kinesigenic dyskinesia. This condition is characterized by episodes of involuntary ... most common genetic change in familial paroxysmal kinesigenic dyskinesia. Most PRRT2 gene variants involved in this condition, ...
    https://medlineplus.gov/genetics/gene/prrt2 - Genetics
  5. DNAI1 gene 
    ... gene have been found to cause primary ciliary dyskinesia, which is a condition characterized by respiratory tract ... cilia lead to the features of primary ciliary dyskinesia. More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/dnai1 - Genetics
  6. ADCY5 gene 
    ... have been identified in people with ADCY5-related dyskinesia, a disorder that causes abnormal involuntary movements. These ... Roze E, Bird TD, Raskind WH. ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations. Neurology. 2015 ...
    https://medlineplus.gov/genetics/gene/adcy5 - Genetics
  7. CSTB gene 
    ... head size (microcephaly), severe developmental delays, abnormal movements (dyskinesia), seizures, and encephalopathy (abnormal brain function). These symptoms ...
    https://medlineplus.gov/genetics/gene/cstb - Genetics
  8. OFD1 gene 
    ... Condition MedlinePlus Genetics provides information about Primary ciliary dyskinesia More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/ofd1 - Genetics
  9. FOXG1 gene 
    ... of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. J Med Genet. 2011 ...
    https://medlineplus.gov/genetics/gene/foxg1 - Genetics
  10. UNC80 gene 
    ... causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations ...
    https://medlineplus.gov/genetics/gene/unc80 - Genetics