SCALP syndrome
ORPHA:370052· ICD-10 Q84.8
Definition
SCALP syndrome is a rare skin disease characterized by the association of sebaceous nevus and aplasia cutis congenita (usually on the scalp and face) in conjunction with limbal dermoid of the eye, a giant congenital melanocytic nevus and variable central nervous system abnormalities, including seizures, hydrocephalus, neurocutaneous melanosis, arachnoid cysts, and diffuse unilateral hemisphere enlargement.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Not applicable
- Age of onset
- Neonatal