11p13 deletion syndrome is a genetic condition caused by the deletion of a small part of chromosome 11, specifically at the short arm (p) in the 13th position. This syndrome can lead to a variety of developmental issues, including intellectual disabilities, growth delays, and distinctive facial features. Individuals with 11p13 deletion syndrome may also experience health problems such as kidney abnormalities and vision issues. The severity and specific symptoms can vary widely among affected individuals, making early diagnosis and personalized care important for managing the condition.