Disparity of child/parent-reported quality of life in cerebral palsy persists into adolescence.
Mariane SentenacMarion RappVirginie EhlingerAllan ColverUte ThyenCatherine ArnaudPublished in: Developmental medicine and child neurology (2020)
The points of view of the child and their parents should be treated as complementary to obtain better knowledge regarding the QoL of children and adolescents with CP.