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درباره پایگاه
فهرست سامانه ها
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فهرست سازمانی
تماس با ما
JCR 2016
جستجوی مقالات
یکشنبه 23 آذر 1404
Dental Research Journal
، جلد ۱۰، شماره ۴، صفحات ۰-۰
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
A rare case of hidebound disease with dental implications
چکیده انگلیسی مقاله
Systemic sclerosis (also called as Scleroderma or hidebound disease) is a chronic sclerotic disease of unknown etiology which causes diffuse, increased deposition of extra cellular matrix in connective tissue with vascular abnormalities, resulting in tissue hypoxia. The disease is characterized by diffuse fibrosis; degenerative changes; and vascular abnormalities in the skin (scleroderma), articular structures, and internal organs. Aesthetic and facial dysfunctions are followed by important oral and facial manifestations. Most oral manifestations begin with tongue rigidity and facial skin changes. Bone resorption of mandibular angle and widening of periodontal ligament space on periapical radiographs are important radiological findings. Other systemic changes include the involvement of internal organs, which lead to serious complications as well as disorders in the cardiac muscle and Raynaud´s phenomenon. This is a case report of 30‑year‑old female patient with the classical features of this disease. This case is reported for its rarity and variable expressivity. The main aim of this article is to describe thorough presentation of the case report, various forms of scleroderma, pathogenesis, oral, extraoral, periodontal manifestations of scleroderma, and its treatment options. A brief review of the literature, focusing on dental alterations is also presented. Key Words: Acroosteolysis, connective tissue, crest syndrome, hidebound disease, periodontitis, Raynaud’s phenomenon, scleroderma
کلیدواژههای انگلیسی مقاله
نویسندگان مقاله
vikram بالی | vikram bali
sarita dabra | sarita dabra
ashima بالی behl | ashima bali behl
rajiv بالی | rajiv bali
نشانی اینترنتی
http://drj.mui.ac.ir/index.php/drj/article/view/1479
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زبان مقاله منتشر شده
en
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Case Report(s)
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