Gastrointestinal Manifestation of Kindler Syndrome
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1. Kindler T. congenital poikiloderma with traumatic bulla formation and progressive cutaneous atrophy. Br J Dermatol 1954; 66: 104-11. 2. Yazdanfar A, Hashemi B. Kindler syndrome: report of three cases in a family and a brief review. Int J Dermatol 2009; 48:145-52. 3. Penagos H, Jaen M, Sancho MT, Saborio MR, Fallas VG, Siegel DH, et al. Kindler syndrome in Native Americans from Panama: report of 26 cases. Arch Dermatol 2004;140:939-44. 4. Lai-Cheong JE, Tanaka A, HawcheG,EmanuelP, Maari C, Taskesen M, et al. Kindler syndrome: a focal adhesion genodermatosis. Br J Dermatol 2009;160: 232-42. 5. Fischer A, Kazandjieva J, Vassileva S, Dourmishev A. Kindler syndrome: a case report and proposal for clinical diagnostic criteria. Acta Dermatovenerol Alp Panonica Adriat 2005;14:61-7. 6. Sadler E, KlauseggerA,Muss W, Deinsberger U, Pohla-Gubo G, Laimer M, et al. Novel KIND1 Gene Mutation in Kindler Syndrome With Severe Gastrointestinal Tract Involvement. Arch Dermatol 2006;142:1619-24. 7. Tulin M, Elcioglu N, Aydingoz I, Deniz A, Asiran Z, Herz C, et al. novel and recurrent KIND1 mutations in two patients with Kindler syndrome and severe mucosal involvement. Acta Derm Venereol 2007;87:563-5. 8. Hirano I, Kahrilas P. Dysphagia. In: Longo DL, Fauci AS, Kasper DL, Harrison”s principles of internal medicine.18th ed. 2012: 297-300. 9. Standards of Practice Committee, Egan JV, Baron TH, Adler DG, Davila R, Faigel DO, et al. Esophageal dilation. Gastrointest Endosc 2006;63:755-60. 10. Ho SB, Cass O, Katsman RJ, Lipschultz EM, Metzger RJ, Onstad GR, et al. Fluoroscopy is not necessary for Maloney dilation of chronic esophageal strictures. Gastrointest Endosc 1995;41:11-4. 11. Hernandez LV, Jacobson JW, Harris MS. Comparison among the perforation rates of Maloney, balloon, and savary dilation of esophageal strictures. Gastrointest Endosc 2000;51:460-2. 12. Wang YG, Tio TL, Soehendra N. Endoscopic dilation of esophageal stricture without fluoroscopy is safe and effective. World J Gastroenterol 2002;8:766-8.
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سندرم Kindler و ارتباط آن با اپیدرمولیز بولوز سیمپلکس: گزارش سه مورد از بیمارستان رازی
Kindler syndrome is characterized by acral blister formation in infancy and childhood, poikiloderma and cutaneous atrophy. Undoubtedly, similarities of the clinical features exist between Kindler syndrome and Epidermolysis bullosa simplex with mottled pigmentation. In this article, we report 3 patients with Kindler syndrome. Until the Bullous component of Kindler syndrome is more completely und...
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Kindler syndrome (KS) is a rare autosomal recessive genodermatosis. We report two cases of KS with classical clinical presentations involving skin and mucus membranes. Clinically, both patients had four major features of KS in the form of acral skin blistering, photosensitivity, progressive poikiloderma, and diffuse cutaneous atrophy. Case 1 had associated features in the form of urethral...
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A 13 years old boy with progressive poikiloderma, bullous lesions in the extremities and photosensitivity is reported. Physical examinations were otherwise normal, his physical development was normal, no other family member had a similar disease. Routin laboratory exams were in the normal limits.Histopathology exams from poikilodermatous skin showed atrophy of the epidermis, liquification degen...
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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 infrequ...
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BACKGROUND Kindler syndrome (online Mendelian Inheritance in Man No. 173650) is an autosomal recessive genodermatosis characterized by acral trauma-induced blistering that improves with age and by progressive poikiloderma in later life. Other clinical features include photosensitivity, webbing of the fingers and toes, nail dystrophy, periodontal disease, and mucosal alterations. Aside from esop...
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