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Williams syndrome - Wikipedia
WEBwilliams syndrome is a microdeletion syndrome caused by the spontaneous deletion of genetic material from the chromosomal region 7q11.23. This is a heterozygous deletion, which results in haploinsufficient expression of the 25–27 genes in this region.
En.m.wikipedia.orgWilliams Syndrome, Williams Beuren Syndrome: Causes, …
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, …
My.clevelandclinic.orgWhat is Williams syndrome?
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.
Williams-syndrome.orgWilliams Syndrome: Symptoms, Diagnosis, and Treatments
WEBJul 9, 2017 · 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
Healthline.comWilliams Syndrome - StatPearls - NCBI Bookshelf
WEBJun 26, 2023 · williams syndrome is a rare genetic disorder with congenital heart disease, distinctive facial features (elfin-like faces), hypercalcemia, neurodevelopmental, and behavioral deficits.
Ncbi.nlm.nih.govWhat is Williams Syndrome? | Overview
WEBwilliams syndrome (WS) is a rare genetic condition that is present at birth. It is caused by a spontaneous genetic deletion of a small stretch of approximately 26-28 adjacent genes on chromosome 7, including the elastin gene, and can affect anyone.
Williamssyndrome.caWilliams Syndrome: Causes, Symptoms, and Diagnosis - WebMD
WEBSep 22, 2024 · 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
Webmd.comWilliams Syndrome | National Institute of Neurological
WEBJul 19, 2024 · What is williams syndrome? 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.
Ninds.nih.govWilliams Syndrome - GeneReviews® - NCBI Bookshelf
WEBApr 9, 1999 · williams syndrome (WS) is a multisystem disorder characterized by cardiovascular disease (elastin arteriopathy, most often manifesting as supravalvar aortic stenosis), developmental delay, usually mild intellectual disability, a specific cognitive profile, unique personality characteristics, connective tissue abnormalities, growth …
Ncbi.nlm.nih.govWilliams syndrome - MedlinePlus
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.
Medlineplus.gov