Pachydermoperiostosis Authors : Doctor M . Auger and Professor

نویسنده

  • N. Stavrianeas
چکیده

Key-words Disease name and synonyms Definition/ Diagnosis criteria History Epidemiology Differential diagnosis Etiology Clinical description Physiopathology Diagnostic methods Genetic counselling Treatment References

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منابع مشابه

Primary Pachydermoperiostosis and report of two cases in a family

Pachydermoperiostosis (PDP) is a rare hereditary disease characterized by folded coarse skin, hyperostosis, clubbing of fingers and abnormalities in other organs such as gastrointestinal tract. Because of safety parents guides us to familial incidence and penetration of gene in 50% of cases. Diagnosis is based on clinical and radiological findings. Males are more susceptible than females to thi...

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[Pachydermoperiostosis (idiopathic hypertrophic osteoarthropathy)].

Introduction Pachydermoperiostosis is a syndrome characterized by finger clubbing, periosteal new bone formation especially over the distal ends of long bones, and coarsening of the facial features, with thickening, furrowing and oiliness of the skin of the face and forehead. The first reported cases were the Hagner brothers, who had typical features of this syndrome. They were first described ...

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تاریخ انتشار 2004