Williams Syndrome is a rare genetic disorder that causes growth and development disorders. This condition is very rare and only occurs in 1 in 10 thousand people. Usually genetic disorders have been known since the baby is born, because there are some "typical" signs that are owned by the sufferer.
Williams syndrome is caused by genetic disorders. However, Williams syndrome can affect anyone, including people who have no history of the disease in their families.
Signs of a Child Suffering from Williams Syndrome
Williams Syndrome is characterized by several distinctive signs and conditions, namely:
1. A unique and distinctive face
Children who have Williams syndrome have a unique and distinctive face, which is a wide forehead, a shorter nose with a wider tip, cheeks that look filled, a wide mouth, and thick lips. When mature, sufferers of Williams syndrome tend to have a longer and thinner face.
2. The condition of teeth that are not normal
Children suffering from Williams syndrome have abnormal tooth growth. Their teeth grow irregularly, small, and tenuous.
3. Slow growth
Newborns with Williams syndrome tend to be underweight. Usually people with this syndrome will experience growth disorders, so that when adults, people with Williams syndrome are generally short posture.
4. Difficulty breastfeeding
Children with Williams syndrome also experience obstacles when eating, such as difficulty swallowing and tendency to eat very slowly.
5. Sensitive hearing
People with Williams syndrome are more sensitive to sound. They can even be surprised when they hear a normal volume sound.
6. Frequent colic
Babies suffering from Williams syndrome more often experience colic. Colic is often associated with hypercalcemia, which is high levels of potassium in the blood, which often occurs in people with Williams syndrome.
7. Slow development
The next sign of Williams syndrome is slow development. Children with Williams syndrome have a delay in talking and walking. Children with Williams syndrome also have the possibility to suffer from ADHD.
8. Heart and blood vessel abnormalities
Patients with Williams syndrome can also have abnormalities in the heart, such as narrowing of the aorta and arteries.
9. Kidney disorders
Although not always, some people with William syndrome can also have abnormalities in the structure and function of the kidneys.
10. Muscle and joint disorders
The next sign of Williams syndrome is an abnormality in the muscles and joints. People with Williams syndrome tend to have weak muscles and poor motion coordination.
In addition to physical abnormalities, patients with low Williams syndrome sufferers also tend to have low intelligence or IQ levels. But they tend to be sociable even not afraid to interact with strangers.
With these various disorders, caring for and assisting children with Williams syndrome is indeed not easy. You must be patient and routinely check his health to the doctor so that his condition is always monitored.
However, you do not need to be discouraged. Although this disorder affects many aspects, children with Williams syndrome are usually quick to learn new things. They can also speak and read well, even some of them have talent in music.
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