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European Journal of Dermatology

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A case of complete form of pachydermoperiostosis with SLCO2A1 mutations Volume 31, numéro 2, March-April 2021

Illustrations


  • Figure 1
Auteurs
Dermatological Department, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing 210008, China

Pachydermoperiostosis (PDP), also referred to as primary hypertrophic osteoarthropathy (PHO), is a rare hereditary disorder characterized by three major symptoms: digital clubbing, pachydermia, and periostosis [1]. Three forms have been categorized: the complete form with pachydermia and periostitis, the incomplete form with evidence of bone abnormalities but lacking pachydermia, and the forme fruste with prominent pachydermia and minimal-to-absent skeletal changes [2]. To date, two genes involving [...]