KINDLER SYNDROME: A CASE REPORT FROM IRAN

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AMIR CHAGHMAGHI MARYAM; MOEINTAGHAVI AMIR; RASEKHI JAVID; MOSANNENMOZAFARI PEGAH; DALIRSANI ZOHREH; JAFARIAN AMIR HOSSEIN

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Journal: JOURNAL OF DENTAL MATERIALS AND TECHNIQUES Year:2014 | Volume:3 | Issue:3 Page(s): 134-138

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Title

KINDLER SYNDROME: A CASE REPORT FROM IRAN

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Keywords

CASE REPORT

GENODERMATOSIS

KINDLER SYNDROME

Abstract

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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APA: Copy

AMIR CHAGHMAGHI, MARYAM, MOEINTAGHAVI, AMIR, RASEKHI, JAVID, MOSANNENMOZAFARI, PEGAH, DALIRSANI, ZOHREH, & JAFARIAN, AMIR HOSSEIN. (2014). KINDLER SYNDROME: A CASE REPORT FROM IRAN. JOURNAL OF DENTAL MATERIALS AND TECHNIQUES, 3(3), 134-138. SID. https://sid.ir/paper/335487/en

Vancouver: Copy

AMIR CHAGHMAGHI MARYAM, MOEINTAGHAVI AMIR, RASEKHI JAVID, MOSANNENMOZAFARI PEGAH, DALIRSANI ZOHREH, JAFARIAN AMIR HOSSEIN. KINDLER SYNDROME: A CASE REPORT FROM IRAN. JOURNAL OF DENTAL MATERIALS AND TECHNIQUES[Internet]. 2014;3(3):134-138. Available from: https://sid.ir/paper/335487/en

IEEE: Copy

MARYAM AMIR CHAGHMAGHI, AMIR MOEINTAGHAVI, JAVID RASEKHI, PEGAH MOSANNENMOZAFARI, ZOHREH DALIRSANI, and AMIR HOSSEIN JAFARIAN, “KINDLER SYNDROME: A CASE REPORT FROM IRAN,” JOURNAL OF DENTAL MATERIALS AND TECHNIQUES, vol. 3, no. 3, pp. 134–138, 2014, [Online]. Available: https://sid.ir/paper/335487/en

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