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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.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? | Williams Syndrome Association
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.comWhat 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
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
Webmd.comWilliams Syndrome Explained - Williams Syndrome Foundation
WEBwilliams syndrome is a rare congenital disorder that occurs randomly and affects around one in 18,000 people in the UK. It is non-hereditary and causes distinctive facial characteristics and a wide range of learning difficulties.
Williams-syndrome.org.ukWilliams Syndrome - National Institute of Neurological Disorders …
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: Features, causes, and treatment - Medical …
WEBMar 23, 2017 · williams syndrome is a rare neurodevelopmental genetic disorder that features mild learning or developmental challenges, a high levels of calcium in the blood and urine, and a markedly
Medicalnewstoday.comWilliams Syndrome Pictures, Signs, Symptoms, Causes & Life Span
WEBwilliams syndrome (also termed Williams-Beuren syndrome) is a rare genetic disorder (in chromosome 7) that results in prenatal and postnatal growth disorder, short stature, variable degrees of mental deficiency and distinctive facial features.
Emedicinehealth.com