Delhi Journal of Ophthalmology

Ophthalmic Features of Schopf-Schulz-Passarge Syndrome

Manpreet Singh, Manpreet Kaur, Aditi Mehta Grewal, Zoramthara Zadeng, Pankaj Gupta
Department of Ophthalmology, Advanced Eye Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Editor-in-Chief, Delhi Journal of Ophthalmology, Dr R.P.Centre, AIIMS.


Corresponding Author:

Manpreet Singh MS, DNB, FAICO
Department of Ophthalmology,
Advanced Eye Centre,
Post Graduate Institute of Medical Education and Research,
Chandigarh, India
Email id: drmanu83@gmail.com


Received: 13-JUL-2019 Accepted: 27-AUG-2019 Published Online: 27-DEC-2019
DOI: https://dx.doi.org/10.7869/djo.487

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