Purpose: To present the ophthalmic manifestations of a 3-month old female with SCALP syndrome.
Observations: The patient presented with multiple ocular anomalies including bilateral limbal dermoids, esotropia and left optic nerve hypoplasia.
Conclusions: We describe systemic and ocular anomalies in a rare case of SCALP syndrome. This report provides additional information on the ocular anomalies not previously described that may be associated with this clinical entity.
Keywords: Aplasia cutis; Limbal dermoid; Melanocytic naevus; Optic nerve hypoplasia; SCALP syndrome; Sebaceous nevus.