Toggle Main Menu Toggle Search

Open Access padlockePrints

A case of Schopf-Schulz-Passarge syndrome

Lookup NU author(s): Dr Brian Angus, Dr Andrew Carmichael


Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


Schopf-Schulz-Passarge syndrome (SSPS) is a rare ectodermal dysplasia characterized by hypodontia, hypotrichosis, nail dystrophy, palmoplantar keratoderma, and periocular and eyelid margin apocrine hidrocystomas. Several other skin tumours have been described in association with this syndrome, in particular, multiple palmoplantar eccrine syringofibroadenoma (ESFA). We report a case of SSPS with diffuse palmoplantar hyperkeratosis, which was shown by histology and immunocytochemistry to be due to ESFA.

Publication metadata

Author(s): Hampton PJ, Angus B, Carmichael AJ

Publication type: Article

Publication status: Published

Journal: Clinical and Experimental Dermatology

Year: 2005

Volume: 30

Issue: 5

Pages: 528-530

ISSN (print): 0307-6938

ISSN (electronic): 1365-2230

Publisher: Blackwell Publishing Ltd


DOI: 10.1111/j.1365-2230.2005.01855.x


Altmetrics provided by Altmetric