Final answer:
Children with Prader-Willi Syndrome need support with motor skills, social interactions, daily activities, and cognitive functions through occupational therapy and the support of family and caregivers.
Step-by-step explanation:
Children with Prader-Willi Syndrome (PWS) require occupational therapy and other therapy services to improve motor skills, social interactions, daily living activities, and cognitive function. These services are vital in assisting them with challenges they may face due to symptoms of PWS, such as balance and posture problems, difficulty with planning and executing tasks, and cognitive deficits. The involvement of their family or caregiver is crucial, especially in managing their diet, behavior, and medical issues to enhance the quality of life for individuals with PWS.
There is no cure for PWS, but treatments aim to manage symptoms and complications. For example, psychoactive medications and growth hormones continue to show promise in addressing certain aspects of PWS. Moreover, genetic testing can be used for diagnosis, and early signs of PWS, such as lack of muscle tone and developmental delays, can inform early intervention strategies.