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Results 1 - 6 of 6 for Dentatorubral pallidoluysian atrophy
  1. ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > Dentatorubral-pallidoluysian atrophy (often shortened to DRPLA ) On this page: Description ...
  2. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... cause Autosomal recessive ataxia of Charlevoix-Saguenay (ARSACS) Dentatorubral-pallidoluysian atrophy (DRPLA) Fragile X tremor-ataxia syndrome (FXTAS) Friedreich's ...
  3. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
  4. Genetics Home Reference: Epilepsy From the National Institutes of Health (National Library of Medicine)  
    ... epilepsy with auditory features benign familial neonatal seizures dentatorubral-pallidoluysian atrophy FOXG1 syndrome guanidinoacetate methyltransferase deficiency hereditary hyperekplexia isodicentric ...
  5. Movement Disorders (National Library of Medicine)  
    Imagine if parts of your body moved when you didn't want them to. If you have a movement disorder, you experience these kinds of impaired movement. Dyskinesia ...
  6. Classification of Ataxia (National Ataxia Foundation)  
    ... SCA30 – Spinocerebellar Ataxia Type 30 Dominant No DRPLA – Dentatorubral-Pallidoluysian Atrophy Dominant Yes FXTAS – Fragile X Tremor-Ataxia X- ...