TY - JOUR ID - 2973 TI - Kindler Syndrome: A case Report from Iran JO - Journal of Dental Materials and Techniques JA - JDMT LA - en SN - 2322-4150 AU - Amirchaghmaghi, Maryam AU - Moeintaghavi, Amir AU - Rasekhi, Javid AU - Mosannen Mozafari, Pegah AU - Dalirsani, Zohreh AU - Jafarian, Amir Hossein Jafarian AD - Oral and Maxillofacial Diseases Research Center, Department of Oral Medicine, School of Dentistry, Mashhad University of Medical Sciences, Mashhad, Iran AD - Dental Material Research Center, Department of Periodontics, School of Dentistry, Mashhad University of Medical Sciences, Mashhad, Iran AD - Department of Pathology, Ghaem Hospital, Mashhad University of Medical Sciences, Mashhad, Iran Y1 - 2014 PY - 2014 VL - 3 IS - 3 SP - 134 EP - 138 KW - case report KW - Genodermatosis KW - Kindler Syndrome DO - 10.22038/jdmt.2014.2973 N2 - 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. UR - https://jdmt.mums.ac.ir/article_2973.html L1 - https://jdmt.mums.ac.ir/article_2973_71f48ea0935cdf6ef7c5e68c6534ba6c.pdf ER -