Schöpf-Schulz-Passarge syndrome

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.