We studied how common pain was thought to be due to muscle spasticity in the legs or arms is in children/adolescents with CP.
The GMFCS can be a helpful tool in clinical and research use and has been shown to be stable and accurate over time. It can also help individuals and families better understand cerebral palsy.
Cohort-based whole exome and whole genome sequencing and copy number variant (CNV) studies have identified genetic etiologies for a sizable proportion of patients with cerebral palsy (CP). These findings indicate that genetic mutations collectively comprise an important cause of CP.
The findings of this article demonstrate the need for improved screening rates in women with CP, and highlight areas for improving their screening experience.