Literature DB >> 25376961

Bilateral ptosis as a presenting feature of primary hypertrophic osteoarthropathy (pachydermoperiostosis): a case report.

S El Aoud1, F Frikha, M Snoussi, R Ben Salah, Z Bahloul.   

Abstract

Pachydermoperiostosis is a rare hereditary disorder, which affects both bones and skin. It is characterized by a combination of dermatologic changes (pachydermia or thickening of the skin) and rheumatologic manifestations (periostosis and finger clubbing). Eyelid ptosis which is caused by thickened eyelids (blepharoptosis) is a less common symptom. We report the case of a patient with a complete form of pachydermoperiostosis with bilateral ptosis as presenting feature.

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Year:  2014        PMID: 25376961     DOI: 10.4081/reumatismo.2014.726

Source DB:  PubMed          Journal:  Reumatismo        ISSN: 0048-7449


  2 in total

1.  Complete primary pachydermoperiostosis: A case report from Jordan and review of literature.

Authors:  Bareqa I Salah; Khalil I Husari; Ala' Hassouneh; Zaid Al-Ali; Baeth Rawashdeh
Journal:  Clin Case Rep       Date:  2019-01-09

2.  Touraine-Solente-Gole syndrome: Clinical manifestation with bilateral true eyelid ptosis.

Authors:  Nutthawut Akaranuchat; Papassorn Limsuvan
Journal:  JPRAS Open       Date:  2019-04-27
  2 in total

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