%0 Journal Article
%T Kindler syndrome: a rare case report from Greece
%A Cristina Has
%A Dimitra Kiritsi
%A Evangelia Kalloniati
%A Maria Gkaitatzi
%A Sophia Georgiou
%A Theofanis Spiliopoulos
%J Archive of "Oxford Medical Case Reports".
%D 2019
%R 10.1093/omcr/omz003
%X Kindler syndrome is a rare autosomal recessive inherited disease characterized by infantile acral bullae, progressive poikiloderma, cutaneous atrophy, photosensitivity and various forms of mucosal involvement. In this paper, we report a case of a 49-year-old Greek Caucasian male aiming to emphasize the importance of genetic analysis as a gold standard of diagnosis
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396407/