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kindler syndrome: a case report from iran
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نویسنده
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amirchaghmaghi maryam ,moeintaghavi amir ,rasekhi javid ,mosannen mozafari pegah ,dalirsani zohreh ,jafarian amir hossein
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منبع
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journal of dental materials and techniques - 2014 - دوره : 3 - شماره : 3 - صفحه:134 -138
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چکیده
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Kindler syndrome (ks) is a rare, autosomal recessive genodermatosis characterized by skin blistering and photosensitivity in infancy, progressive poikiloderma, and diffuse cutaneous atrophy. it affects the skin, mucous membranes, and oral cavity and is caused by mutations in the kind1 gene on 20p12.3. the first case of ks associated with periodontitis was reported in 1996, and have been infrequently reported since. here we present a case of ks with classic clinical presentations involving skin, mucous membranes, and the periodontium in a patient from iran.
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کلیدواژه
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case report ,genodermatosis ,kindler syndrome
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آدرس
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mashhad university of medical sciences, oral and maxillofacial diseases research center, school of dentistry, department of oral medicine, ایران, mashhad university of medical sciences, dental material research center, school of dentistry, department of periodontics, ایران, mashhad university of medical sciences, oral and maxillofacial diseases research center, school of dentistry, department of oral medicine, ایران, mashhad university of medical sciences, oral and maxillofacial diseases research center, school of dentistry, department of oral medicine, ایران, mashhad university of medical sciences, oral and maxillofacial diseases research center, school of dentis, department of oral medicine, ایران, mashhad university of medical sciences, ghaem hospital, department of pathology, ایران
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Authors
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