Schöpf-Schulz-Passarge syndrome

MONDO:0009145

A rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy.

Also known as: SSPS, eccrine tumors-ectodermal dysplasia, keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome, palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome, palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome, SCHOPF-Schulz-Passarge syndrome, SChöPF-Schulz-Passarge syndrome, eccrine tumors with ectodermal dysplasia

7 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Syndromic disease (24) Human disease (14) Hereditary skin disorder (5) Autosomal recessive disease (4) Palmoplantar keratosis (4) Ectodermal dysplasia syndrome (3) Keratosis (3)

Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1

Skin deep: european study probes the hidden emotional toll of skin diseases

Knowledge-focused Not yet recruiting

This study looks at how people with skin conditions (like eczema, psoriasis, or skin cancer) manage stress, feel lonely, and bounce back from challenges. Researchers will compare 375 adults with and without skin disease across 15 European countries using questionnaires. The goal …

Phase: NA • Sponsor: University Hospital, Brest • Aim: Knowledge-focused

Last updated Jun 27, 2026 13:06 UTC

Schöpf-Schulz-Passarge syndrome

Broader categories

Skin deep: european study probes the hidden emotional toll of skin diseases