It’s SMART to think about what you might want to discuss at your next doctor’s appointment. Here are some suggestions
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.
This fact sheet is a sexual and reproductive health guideline for providers treating young women with cerebral palsy.
Oropharyngeal dysphagia, or OPD, is an impairment of the oral or pharyngeal phases of the swallow. This can impair muscle movements and coordination of the mouth, such as the lips, tongue, jaw, cheeks, palate, and also muscles of the pharynx and the entry to the airway.
The typical cognitive assessments that are used for children require them to be able to use their hands to point to pictures or hold puzzle pieces.
It’s SMART to think about what you might want to discuss at your next doctor’s appointment. Here are some suggestions
For a child with CP learning to move, the really important things to remember are that the child should always be active.
To give you an idea about genetic variation between each of us, there are about three million differences in our genetic code. They go to influence the color of our hair and the color of our eyes, the way we walk.