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Williams syndrome is a rare genetic condition which can give a person special facial features, a sociable personality, and some learning challenges. Williams Syndrome is a rare genetic disorder with characteristic features, signs, and symptoms like digestive and eye problems, low birth weight, and cardiac abnormalities. Symptoms of Williams syndrome can be treated, but there is no cure. Williams Syndrome is a genetic disorder characterized by developmental delays and certain medical conditions such as heart problems and low muscle tone. Life-span for Williams syndrome is age 10-20. It can also affect a child's ability to learn. Williams syndrome is inherited and sometimes spontaneous. People with Williams syndrome also often have advanced language skills, outgoing personalities, and a love for music. In a small percentage of cases, people with Williams syndrome inherit the chromosomal deletion from a parent with the condition. In most cases, the gene changes (mutations) occur on their own, either in the sperm or egg that a … It is caused by a chromosome abnormality and affects how a person grows and develops. Facial Features. Williams syndrome can cause symptoms in different parts of the body, such as the face, heart, and other organs. Williams syndrome is considered an autosomal dominant condition because one copy of the altered chromosome 7 in each cell is sufficient to cause the disorder. Williams syndrome is caused by not having a copy of 25 to 27 genes on chromosome number 7. Problems with chromosome 7 causes the condition.