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Williams Syndrome is a rare genetic disorder with characteristic features, signs, and symptoms like digestive and eye problems, low birth weight, and cardiac abnormalities. Williams syndrome is inherited and sometimes spontaneous.
1 Μαΐ 2008 · Signs & Symptoms. Williams syndrome is characterized by a wide spectrum of symptoms and physical features that vary greatly in range and severity, even among affected family members. Individuals with Williams syndrome will not have all the symptoms listed below.
23 Μαρ 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 outgoing...
22 Σεπ 2024 · Some common signs of Williams syndrome include: Unique personality; Unique facial features; Chronic ear issues; Being very sensitive to sound; Heart problems; Attention deficit hyperactivity...
22 Οκτ 2024 · This article will explore the prevalence, causes, signs and symptoms, diagnosis, treatment, and latest research on Williams Syndrome. Causes of Williams Syndrome. Large gene deletions from a specific band on the long arm of chromosome 7 cause Williams Syndrome.
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.
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 "deletion").
