Skip navigation

Refine by Type

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. 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- ...
  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. 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 ...