Schöpf–Schulz–Passarge syndrome (Q7433355)
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SchC6pf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy
- Palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome
- SSPS
- Palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome
- Schöpf-Schulz-Passarge syndrome
- Eccrine tumors-ectodermal dysplasia
- Eccrine Tumors With Ectodermal Dysplasia
- Keratosis Palmoplantaris With Cystic Eyelids, Hypodontia, and Hypotrichosis
- Keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome
- SCHOPF-SCHULZ-PASSARGE SYNDROME
- SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS
- Schopf-Schulz-Passarge syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Schöpf–Schulz–Passarge syndrome |
SchC6pf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy |
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Wikipedia(3 entries)
- dewiki Schöpf-Schulz-Passarge-Syndrom
- enwiki Schöpf–Schulz–Passarge syndrome
- trwiki Schopf-Schulz-Passarge sendromu