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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. Problems with chromosome 7 causes the condition. Symptoms of Williams syndrome can be treated, but there is no cure. Life-span for Williams syndrome is age 10-20.
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Dec 10, 2021 · Symptoms of Williams syndrome include: Chronic ear infections and/or hearing loss. Dental abnormalities, such as poor enamel and small or missing teeth. Elevated calcium level in the blood. Endocrine abnormalities: hypothyroidism, early puberty and diabetes in adulthood. Farsightedness. Feeding difficulties in infancy.
- Williams syndrome is a genetic condition characterized by unique facial features, delayed development, learning problems, and certain personality t...
- Williams syndrome is caused by a deletion, or missing piece, of a region on chromosome 7. Some important points to know about this genetic conditio...
- Williams syndrome may cause a range of developmental issues and symptoms. The condition is typically diagnosed in infancy or early childhood. Not a...
Jul 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 mouth ...
Williams 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. Infants often have delayed development and can develop physical and mental health problems, including anxiety and ...
Williams syndrome (WS), also Williams–Beuren syndrome (WBS), is a genetic disorder that affects many parts of the body. [ 2 ] Facial features frequently include a broad forehead, underdeveloped chin, short nose, and full cheeks. [ 2 ] Mild to moderate intellectual disability is observed, particularly challenges with visual spatial tasks such ...
May 1, 2008 · Symptoms may include loss of appetite (anorexia), irritability, confusion, weakness, easy fatigability, and/or abdominal and muscle pain. Some studies in the medical literature question whether idiopathic infantile hypercalcemia is a separate disorder from Williams Syndrome or if it is a variant of the same disease.
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Individuals with Williams syndrome are described as having similar facial features. These features include a small upturned nose, long philtrum (upper lip length), wide mouth, full lips, small chin, and puffiness around the eyes. Blue and green-eyed individuals with Williams syndrome can have a prominent "starburst" or white lacy pattern on ...
