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An. bras. dermatol ; 95(1): 98-101, Jan.-Feb. 2020. graf
Article Dans Anglais | LILACS | ID: biblio-1088724

Résumé

Abstract Pachydermoperiostosis (PDP) or primary hypertrophic osteoarthropathy (PHO) is a rare hereditary disease characterized by digital clubbing, pachydermia, and periostosis. Its pathogenesis is uncertain and the diagnosis is based on clinical and radiological data. A complete form of the syndrome is reported in a male patient with disease onset in adolescence, with compatible clinical and radiological findings, presenting the three cardinal findings as well as other associated manifestations, such as hyperhidrosis and acne.


Sujets)
Humains , Mâle , Jeune adulte , Pachydermopériostose/anatomopathologie , Dermatoses du cuir chevelu/anatomopathologie , Érythème/anatomopathologie
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