Undersökning av muskel- och andningsfunktion hos barn med SMA som behandlas med nusinersen (Spinraza)

  • Dereksson, Kristján (Forskarstuderande)
  • Eklund, Erik (Handledare)
  • Rönne Hansen, Christine (Biträdande handledare)
  • Markström, Agneta (Biträdande handledare)
  • Lindblad, Anders (Biträdande handledare)

Projekt: Avhandling

Projektinformation

Beskrivning

Spinal Muscle Atrophy is a genetic disease that usually presents in childhood. Recently a treatment for the disease, nusinersen, was found to be effective in slowing down or stopping the disease progression. In our study we will be measuring how respiratory function, muscle function and quality of life change over the course of 5 years after treatment start with nusinersen.

Populärvetenskaplig beskrivning

Spinal Muscle Atrophy is a genetic disease that usually presents in childhood. Recently a treatment for the disease was found to be effective in slowing down or stopping the disease. In our study we will be measuring how muscle function and breathing function changes over time in children who receive the new treatment.
Kort titelSMA andningsstudie
StatusPågående
Gällande start-/slutdatum2019/12/012024/12/31

Samarbetspartner

  • Lunds universitet (huvudsaklig)
  • Karolinska University Hospital
  • Queen Silvia Children’s Hospital
  • Uppsala University Hospital