Wolf-Hirschhorn Syndrome is a rare genetic disorder caused by a deletion of genetic material on chromosome 4. It is characterized by a range of physical and developmental challenges, including growth delays, intellectual disabilities, and distinctive facial features such as a broad forehead and a prominent nose. Individuals with Wolf-Hirschhorn Syndrome may also experience seizures, hearing loss, and other health issues. Early intervention and supportive therapies can help improve quality of life, but the severity of symptoms can vary widely among affected individuals.