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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.
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.
29 Αυγ 2021 · The most common symptoms of Williams syndrome are: Chronic middle ear infections. Congenital heart defects. Delays in motor development. “Elfin-like” facial features. Extreme sensitivity to sound. Mild intellectual disability.
9 Ιουλ 2017 · Common symptoms of the condition include: specific facial features like a wide mouth, small upturned nose, widely spaced teeth, and full lips. colic or feeding problems. attention deficit...
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...
23 Μαρ 2017 · Features. Causes and diagnosis. Treatment. Outlook. Williams syndrome is a rare neurodevelopmental genetic disorder that features mild learning or developmental challenges, a high levels of...
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.
