Difficulty: Moderately Challenging
Things You’ll Need:
- Family history
- Support group
- Eyeglasses
- Kidney ultrasounds
- Physical therapy
- Blood tests
- Antibiotics
Step1
Gather your family's medical history. Those with a family history of Williams Syndrome are much more likely to pass it on as a hereditary condition. Those with the syndrome themselves have a 50/50 chance of passing it to their children.
Step2
Have your doctor examine your child closely if you suspect Williams Syndrome. The most common signs include a noticeable, star-like pattern occurring in the iris of the eye, cognitive and developmental problems, large lips and "mouth breathing," difficulty feeding, joint problems and a small stature when compared to other close relatives.
Step3
Treat the symptoms of Williams Syndrome as they arise, because there is no cure for the condition itself. You will need to monitor your child's condition closely to look for signs of recurring problems, because your child most likely will not be able to monitor his own health.
Step4
Test your child's blood often for blood calcium levels. High blood calcium is one of the most common symptoms of Williams Syndrome and is potentially very dangerous. Avoid calcium supplements and foods containing vitamin D.
Step5
Have your child's blood pressure checked regularly. A narrowing of the aorta and blood vessels is common for those with Williams Syndrome and can lead to serious heart problems. Hypertension is a serious complication associated with this condition.
Step6
Get a kidney ultrasound periodically as recommended by your doctor. Renal defects and infection are another common problem for Williams syndrome sufferers. Treat infections with antibiotics and keep an eye out for kidney stones.
Step7
Use glasses to treat the farsightedness that often accompanies Williams Syndrome.
Step8
Engage in physical therapy to help treat problems of the joints and muscles, and have a therapist work with your child on developmental and speech issues.