Schöpf-Schulz-Passarge syndrome
Schöpf-Schulz-Passarge syndrome
Clinical features Schöpf-Schulz-Passarge syndrome is an autosomal recessive tricho-odonto- onycho-dermal dysplasia that shares dental anomalies, a diffuse palmoplantar keratoderma, and nail dystrophy (Fig. 3.110).1–2 Schöpf-Schulz-Passarge syndrome features hypotrichosis, nail fragility, early loss of deciduous teeth, hydrocystomas of the eyelids (Fig. 3.111) or other follicular and adnexal, mostly benign, tumors occurring in older patients.1–5 The diffuse palmoplantar keratoderma has a late onset.1–5
Fig. 3.110 Schöpf-Schulz-Passarge syndrome: diffuse keratoderma on palms and fingers is associated with nail dystrophy.
Fig. 3.111 Schöpf-Schulz-Passarge syndrome: multiple yellowish and bluish cysts on the eyelids.