Also known as: Williams-Beuren syndrome.
What is Williams syndrome?
Williams syndrome is a rare genetic disorder that causes short stature, developmental delay, unique facial features and growth delays, among many other symptoms including heart problems.
What causes Williams syndrome?
Williams syndrome is caused by a genetic mutation. In most cases, this mutation occurs randomly for no known reason, though it can also be hereditary and passed along from parents to children.
What are the symptoms of Williams syndrome?
A wide range of different symptoms can occur with Williams syndrome. Some of the symptoms include:
What are Williams syndrome care options?
There is no cure for Williams syndrome. Different medications, therapies and surgeries may be appropriate treatment depending on which of the many different symptoms are present with the disease.
Reviewed by: Parul B Jayakar, MD
This page was last updated on: December 18, 2020 05:06 PM
Learn more about
Congenital Heart Defects/Disease
Any unusual physical feature or health problem that is present at the birth of a baby is known as a birth defect or a congenital anomaly.
Whenever a child fails to reach a set of developmental milestone for physical/motor, in language and communication, social, or behavioral function, and/or cognitive ability at their expected time, it's known as developmental delay.