Williams Syndrome, Williams Beuren Syndrome: Causes, …
Williams syndrome, also known as Williams-Beuren syndrome, is a rare, neurodevelopmental, genetic condition characterized by many symptoms including unique physical features, delayed development, cognitive challenges and cardiovascular abnormalities.
What is Williams syndrome?
Williams syndrome (WS) is a genetic condition that is present at birth and can affect anyone. It is characterized by medical problems, including cardiovascular disease, developmental delays, and learning challenges.
Williams syndrome - Wikipedia
Williams syndrome is caused by a genetic abnormality, specifically a deletion of about 27 genes from the long arm of one of the two chromosome 7s. [2][4] Typically, this occurs as a random event during the formation of the egg or sperm from which a person develops. [2] .
Williams Syndrome: Causes, Symptoms, and Diagnosis - WebMD
2024年9月22日 · Williams syndrome (WS), also called Williams-Beuren syndrome (WBS), is a rare genetic disorder that causes a variety of symptoms throughout the body. If your child's …
Williams syndrome - MedlinePlus
Williams syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by mild to moderate intellectual disability or learning problems, unique personality characteristics, distinctive facial features, and heart and blood vessel (cardiovascular) problems.
Williams Syndrome: Symptoms, Diagnosis, and Treatments
2017年7月9日 · Williams syndrome, also called Williams-Beuren syndrome, is a rare genetic disorder. It causes many developmental problems. These can include heart and blood vessel issues...
Williams Syndrome - Boston Children's Hospital
Williams syndrome is caused by a change in the amount of an individual’s genetic make-up, or DNA. DNA is found in the form of structures called chromosomes. Williams syndrome occurs when a child has a small deletion or missing piece of one of their chromosomes, called chromosome 7.