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

0 clinical trials for this condition and its sub-types, 0 tagged with Schöpf-Schulz-Passarge syndrome itself.

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↑ Autosomal recessive disease (994) ↑ Diffuse palmoplantar keratoderma (12) ↑ Ectodermal dysplasia WNT10A related (2)

Including sub-types (0) Tagged with Schöpf-Schulz-Passarge syndrome (0)

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