Ophthalmic Features of Schopf-Schulz-Passarge Syndrome

Abstract

Schopf–Schulz–Passarge syndrome (SSPS) is an ectodermal dysplasia of autosomal recessive inheritance. The SSPS involves two or more of the following structures: sweat glands, hair, teeth, nails, and other ectodermal structures. The features of this syndrome constitute multiple periocular and eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypodontia, hypotrichosis, and nail dystrophy. We present pictorial description of the SSPS.

Keywords

• eccrine hidrocystoma of eyelid
• eyelid translucent cysts
• apocrine hidrocystomas
• schopf-schulz-passarge syndrome