70 top medical experts on Schopf-Schulz-Passarge Syndrome across 12 countries and 1 U.S. states, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Schopf-Schulz-Passarge Syndrome: Schöpf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: Eccrine Tumors With Ectodermal Dysplasia, And Hypotrichosis Hypodontia Keratosis Palmoplantaris With Cystic Eyelids
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