Catalog

Schöpf-Schulz-Passarge syndrome

No MMS code

Link to WHO Definition

Schöpf-Schulz-Passarge syndrome – http://id.who.int/icd/entity/441760957

Schöpf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterised by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy.