Williams syndrome is a genetic disorder that affects approximately one in 25,000 births. Early intervention is the key to a long lifespan with this disease and can it also improve quality of life. Read more: What Is the Life Expectancy of Someone with Williams Syndrome? Article
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Related Disease Conditions
Genetic Diseases (Disorder Definition, Types, and Examples)
The definition of a genetic disease is a disorder or condition caused by abnormalities in a person's genome. Some types of genetic inheritance include single inheritance, including cystic fibrosis, sickle cell anemia, Marfan syndrome, and hemochromatosis. Other types of genetic diseases include multifactorial inheritance. Still other types of genetic diseases include chromosome abnormalities (for example, Turner syndrome, and Klinefelter syndrome), and mitochondrial inheritance (for example, epilepsy and dementia).
Williams syndrome is a developmental disorder that affects many parts of the body. Signs, symptoms, characteristics and features may include intellectual disability, learning problems, unique personality characteristics, distinctive facial features, and heart and blood vessel problems. Williams syndrome is a genetic condition that involves chromosome 7.
Your health care provider may refer you to a genetic professional. Universities and medical centers also often have affiliated genetic professionals, or can provide referrals to a genetic professional or genetics clinic. Genetic counseling provides patients and family members the tools to make the right choice in regard to test for a disease or condition.
Is Williams Syndrome the Same as Down Syndrome?
How do I tell the difference between Williams syndrome and Down syndrome? Learn causes, symptoms, and treatments for both.
Who Should Get Genetic Counselling?
Genetic counseling is the process that helps you in determining hereditary or genetic (running in your family) problems that might affect you or your family. It is done by a trained professional.