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Williams Syndrome, Williams Beuren Syndrome: Causes, …
https://my.clevelandclinic.org/health/diseases/15174-williams-syndrome
WebDec 10, 2021 · 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. Williams syndrome may cause poor growth in childhood, and most adults …
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Williams syndrome - Wikipedia
https://en.wikipedia.org/wiki/Williams_syndrome
WebWilliams syndrome (WS), also Williams–Beuren syndrome (WBS), is a genetic disorder that affects many parts of the body. Facial features frequently include a broad forehead, underdeveloped chin, short nose, and full cheeks.
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What is Williams syndrome? | Williams Syndrome Association
https://www.williams-syndrome.org/what-is-ws
WebWilliams 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. These often occur side by side with striking verbal abilities, highly social personalities, and an affinity for music.
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Williams Syndrome | Boston Children's Hospital
https://www.childrenshospital.org/conditions/williams-syndrome
WebWilliams syndrome is a rare (affecting 1 in 10,000 people) developmental disorder that can affect many parts of the body, including the heart and blood vessels. Children with Williams syndrome have mild to moderate intellectual disability, distinctive facial features, and an outgoing personality.
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Williams Syndrome: Causes, Symptoms, and Diagnosis - WebMD
https://www.webmd.com/children/williams-syndrome
WebAug 3, 2022 · Williams syndrome is a rare genetic disorder that causes a variety of symptoms and learning issues. Children with this syndrome could have problems with their heart, blood vessels, kidneys, and...
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Williams Syndrome - National Institute of Neurological Disorders and Stroke
https://www.ninds.nih.gov/health-information/disorders/williams-syndrome
WebNov 28, 2023 · Williams syndrome (WS) is a rare genetic disorder. People with WS may have mild to moderate delays in their cognitive development (ability to think and reason) or learning difficulties. They also may have a distinctive facial appearance, and a unique personality that combines over-friendliness and high levels of empathy with anxiety.
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Williams syndrome: MedlinePlus Genetics
https://medlineplus.gov/genetics/condition/williams-syndrome/
WebWilliams 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.
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Williams syndrome - About the Disease - Genetic and Rare …
https://rarediseases.info.nih.gov/diseases/7891/williams-syndrome/
WebWilliams syndrome is a genetic condition that affects many parts of the body. Signs and symptoms include mild to moderate intellectual disability; unique personality traits; distinctive facial features; and heart and blood vessel problems. Williams syndrome is caused by a person missing more than 25 genes from a specific area of chromosome 7 (a ...
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Williams syndrome Information | Mount Sinai - New York
https://www.mountsinai.org/health-library/diseases-conditions/williams-syndrome
WebWilliams syndrome is a rare disorder that can lead to problems with development. Causes. Williams syndrome is caused by not having a copy of 25 to 27 genes on chromosome number 7. In most cases, the gene changes (mutations) occur on their own, either in the sperm or egg that a baby develops from.
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Williams Syndrome: Symptoms, Diagnosis, and Treatments - Healthline
https://www.healthline.com/health/williams-syndrome
WebJul 9, 2017 · Williams syndrome is a condition made up of specific symptoms that significantly impact health and development. Common symptoms of the condition include: specific facial features like a wide...
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