William Syndrome

William Syndrome is a rare genetic condition caused by the deletion of about 26 genes from a specific region on chromosome 7. It results in distinctive facial features, cardiovascular problems, and unique cognitive profiles. People with William Syndrome often have strong verbal skills and social personality, making them friendly and open, but may face challenges with spatial reasoning, coordination, and learning new tasks. The condition is present at birth and requires ongoing medical and educational support to help individuals reach their full potential.