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Genetic rhabdomyolysis within the spectrum of the Spinocerebellar Ataxia type 2 responsive to pregabalin.

Fabian RossiJoe MaNina TsakadzeLourdes Benes-LimaJulio Araque GonzalezMichael Hoffmann
Published in: Cerebellum & ataxias (2021)
This is the first report of Spinocerebellar Ataxia type 2 associated with chronic, severe, recurrent rhabdomyolysis as part of its genetic phenotype responsive to pregabalin.
Keyphrases
  • acute kidney injury
  • early onset
  • neuropathic pain
  • genome wide
  • cancer therapy
  • copy number
  • postoperative pain
  • drug induced
  • gene expression
  • dna methylation
  • spinal cord