WS can cause a set of symptoms that may occur together. Williams syndrome is inherited and sometimes spontaneous.
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The condition becomes apparent as the child gets older.
Williams syndrome symptoms. Williams syndrome is characterized by certain manifestations including distinctive facial features cardiovascular anomalies elevated levels of calcium in the blood hypercalcemia developmental delays cognitive motor and social and specific behavioral patterns. Additional signs and symptoms of Williams syndrome include abnormalities of connective tissue tissue that supports the bodys joints and organs such as joint problems and soft loose skin. People with Williams syndrome often have certain facial characteristics that are distinct and unique to the syndrome.
So it differs from one person to another. Symptoms Of Williams Syndrome. You may not see any signs at the birth of the child.
Affected people may also have increased calcium levels in the blood hypercalcemia in infancy developmental delays problems with coordination and short stature. People affected by the syndrome may not have the same symptoms. Sings and symptoms of Williams syndrome include distinct facial features broad forehead short nose with a broad tip full cheeks wide mouth with full lips and dental problems People with Williams syndrome frequently develop aortic stenosis high blood pressure and other cardiac and connective tissue related problems and hypercalcemia.
Williams Syndrome Symptoms Signs and symptoms of this disorder include the following. One of the more serious features of Williams syndrome is cardiovascular disease. Williams Syndrome is a rare genetic disorder with characteristic features signs and symptoms like digestive and eye problems low birth weight and cardiac abnormalities.
Speech which is delayed but later might turn into strong speaking and learning abilities by hearing. Not all people with Williams syndrome will have the same set of symptoms. Narrowing of various blood vessels is common especially peripheral pulmonic stenosis and supravalvular aortic stenosis which can lead to increased blood pressure arrhythmia irregular heartbeat and ultimately cardiac failure.
It is non-hereditary and causes distinctive facial characteristics and a wide range of learning difficulties. Many authors such as González Fernández and Uyaguari Quezada 2016 describe the clinical spectrum of Williams syndrome categorized in several areas. Mild to moderate.
Young children tend to have broad foreheads short noses full cheeks and a wide mouth with full lips. Signs and symptoms. The Williams syndrome like other pathologies of genetic origin presents a clinical course characterized by a multisystem affectation.
Once teeth come in they may be crooked small widely spaced or missing. The signs and symptoms of Williams syndrome can vary but generally include. Williams Syndrome is a rare congenital disorder that occurs randomly and affects around one in 18000 people in the UK.
