Link: https://en.wikipedia.org/wiki/Williams_syndrome
Description: 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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Link: https://my.clevelandclinic.org/health/diseases/15174-williams-syndrome
Description: 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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Link: https://www.williams-syndrome.org/what-is-ws
Description: 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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Link: https://www.webmd.com/children/williams-syndrome
Description: 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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Link: https://medlineplus.gov/genetics/condition/williams-syndrome/
Description: 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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Link: https://www.ninds.nih.gov/health-information/disorders/williams-syndrome
Description: 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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Link: https://www.healthline.com/health/williams-syndrome
Description: 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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Link: https://www.ncbi.nlm.nih.gov/books/NBK544278/
Description: WEBNov 7, 2019 · Williams syndrome (WS) is a rare genetic and neurodevelopmental disorder. WS often presents at birth when the child is discovered to have supra-vascular aortic stenosis. The child also shows distinctive facies (elfin-like features), hypercalcemia, connective tissue abnormalities, growth abnormalities, intellectual disability, behavior …
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Link: https://www.childrenshospital.org/conditions/williams-syndrome
Description: 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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Link: https://www.mountsinai.org/health-library/diseases-conditions/williams-syndrome
Description: 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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