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Chromosome Microarray Analysis for the Investigation of Deletions in Pediatric Movement Disorders: A Systematic Review of the Literature.

Luca SolianiAdrián Alcalá San MartínSol BalsellsCristina Hernando-DavalilloJuan Dario Ortigoza-Escobar
Published in: Movement disorders clinical practice (2023)
Our results support the use of CMA as an investigational test in children with movement disorders. As the majority of identified articles were case reports and small case series (low quality), future efforts should focus on larger prospective studies to examine the causation of microdeletions in pediatric movement disorders.
Keyphrases
  • young adults
  • gene expression
  • quality improvement
  • case report
  • dna methylation
  • study protocol
  • open label
  • data analysis