People with Williams syndrome also often have advanced language skills, outgoing personalities, and a love for music. Williams Syndrome is a rare genetic disorder with characteristic features, signs, and symptoms like digestive and eye problems, low birth weight, and cardiac abnormalities.

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