Williams Contiguous Gene Syndrome, also known as WCAGS, is a rare genetic disorder that affects multiple systems of the body. This condition is characterized by deletions on chromosome 7, resulting in the loss of certain genes. Individuals with WCAGS often experience intellectual disability, distinctive facial features, cardiovascular issues, and growth abnormalities. Synonyms for WCAGS include Williams-Beuren Syndrome, Williams Syndrome, and Elastin Deletion Syndrome. These terms are commonly used interchangeably to describe this genetic disorder. While the condition manifests differently in each individual, early diagnosis and intervention are crucial in managing the symptoms and providing the necessary support for individuals living with WCAGS.