Kindler syndrome: a rare case report from Greece

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Kindler Syndrome: A case Report from Iran

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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kindler syndrome: a case report from iran

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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Report of a Case Report of Kindler Syndrome

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: 2 Case Reports from India

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Visceral leishmaniasis during pregnancy: A rare case report from Greece

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ژورنال

عنوان ژورنال: Oxford Medical Case Reports

سال: 2019

ISSN: 2053-8855

DOI: 10.1093/omcr/omz003