DIAGNOSIS
Willi-Prader syndrome is usually suspected based on indications and symptoms. A blood test can almost always provide a definite diagnosis. Aside from that, genetic testing can also detect chromosome abnormalities that indicate this syndrome in your child.
TREATMENT
People with Willi-Prader syndrome can benefit from early diagnosis and treatment, enhancing their quality of life. To manage the disease, you will most likely engage with a group of health specialists.
A hormone disorder specialist, behavior specialists, a dietitian, physical or occupational therapist, a psychiatrist, a geneticist, and other specialists as needed may be part of the team.
Although particular treatments vary depending on the severity of the symptoms, many kids with Willi-Prader syndrome will require the following:
- Mental health care
- Behavior management
- Therapies
- Treatment of sleep disturbances
- Good nutrition for infants
- Weight management
- Sex hormone treatment
- Human growth hormone treatment
Consult your doctor about the treatment options for your child’s condition.