What syndrome is identified with neurocutaneous involvement?

Sturge-Weber syndrome is identified with neurocutaneous involvement due to its distinctive association with both neurological abnormalities and cutaneous manifestations. This syndrome is characterized by a facial birthmark known as a port-wine stain, which is typically found in the distribution of the trigeminal nerve. In addition to the cutaneous effects, individuals with Sturge-Weber syndrome often experience neurological issues such as seizures, developmental delays, and various forms of cognitive impairment. The underlying pathology of this syndrome includes a vascular malformation of the brain that can lead to atrophy and calcification, further linking the skin changes to neurological symptoms. Hence, it is categorically recognized as a neurocutaneous syndrome, making it the correct answer.