Long ‐term dental management of a patient with features of Schöpf–Schulz–Passarge syndrome

ABSTRACT
Schöpf–Schulz–Passarge syndrome (SSPS) is thought to be a rare autosomal recessive condition similar to many other ectodermal dysplasias. Diagnosis is difficult, with many possible differential diagnoses; however, eyelid cysts are a commonly seen feature. This clinical report aims to highlight this and describe the dental features and management of this syndrome, which existing literature has not previously described.

Source: Special Care in Dentistry - May 1, 2017 Category: Dentistry Authors: Nandika Manchanda, Robert Anthonappa, Hessa Al ‐Mulla, Nigel King Tags: CASE HISTORY REPORT Source Type: research