Surgical Treatment of Primary Pachydermoperiostosis: Report of Two Cases
نویسندگان
چکیده
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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15 صفحه اول[Primary hypertrophic osteoarthropathy (pachydermoperiostosis). Report of two familial cases and literature review].
The primary hypertrophic osteoarthropathy (pachydermoperiostosis) is a hereditary disease characterized by skin thickening (pachydermia), finger clubbing, and proliferation of periosteum (periostitis) with subperiosteal new bone formation. We describe the cases of two brothers of 30 and 24 years, who consulted due to bone pain, arthralgia and oligoarthritis. Pachydermia, hyperhidrosis, seborrhe...
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AIM Impaction of deciduous teeth is an uncommon event. The purpose of this report is to describe two unusual eruption failures of a second primary molar and their treatment management. CASE REPORT The diagnostic and therapeutic protocol of two cases selected at the Unit of Paediatric Dentistry, Department of Oral and Maxillofacial Science, "Sapienza" University of Rome, Italy, are presented. ...
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Introduction: Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is a rare disorder in women which identified as agenesis of vagina and hypoplasia or agenesis of uterine. Case presentation: in this study, two female cases (17, and 19 years old) diagnosed with MRKH (first one type 2, and second one type 1) are described. Both patients were presented with amenorrhea, and absence of vagina orifice. On...
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ژورنال
عنوان ژورنال: Revista Brasileira de Cirurgia Plástica (RBCP) – Brazilian Journal of Plastic Sugery
سال: 2014
ISSN: 2177-1235
DOI: 10.5935/2177-1235.2014rbcp0027