Keratosis palmoplantaris papulosa View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2012-05

AUTHORS

C. Mühlhoff, M. Megahed

ABSTRACT

Keratosis palmoplantaris punctata (KPPP) is a rare genodermatosis inherited in autosomal dominant fashion. Clinical findings are multiple, hyperkeratotic, mostly asymptomatic, pinhead-sized papules localized on the palms and soles with progression to hyperkeratotic plaques at pressure sites. A 79-year-old woman presented with a history of hyperkeratotic papules on the palms and soles. Clinical and histopathologic criteria led to the diagnosis KPPP. Identification of causative genes is necessary to permit a better classification and estimation of associated disorders. More... »

PAGES

368-369

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00105-012-2375-2

DOI

http://dx.doi.org/10.1007/s00105-012-2375-2

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1007239559

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/22527298


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