Abstract
Schopf–Schulz–Passarge syndrome (SSPS) is a rare type of ectodermal dysplasia characterized by palmoplantar keratoderma, hypodontia, hypotrichosis, nail dystrophy and multiple periocular and eyelid apocrine hidrocystomas. A 23-year-old female presented with eyelid hidrocystomas, palmoplantar keratoderma, nail dystrophy and thin scalp hair. Skin biopsy was consistent with apocrine hidrocystoma. The patient was diagnosed with SSPS.
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Corresponding Author
Ravinder Singh
Medical Officer, Dermatology DR RKGMC Hamirpur H.P India
DOI: https://dx.doi.org/10.18535/jmscr/v8i6.57
