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Kindler syndrome
Kindler syndrome (also known as "Bullous acrokeratotic poikiloderma of Kindler and Weary,", "Congenital poikiloderma with blisters and keratoses,"〔 "Congenital poikiloderma with bullae and progressive cutaneous atrophy,"〔 "Hereditary acrokeratotic poikiloderma,"〔 "Hyperkeratosis–hyperpigmentation syndrome,"〔Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.〕 "Acrokeratotic poikiloderma," and "Weary–Kindler syndrome"〔James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0-7216-2921-0.〕) is a rare congenital disease of the skin caused by a mutation in the KIND1 gene.
==Diagnosis==
Infants and young children with Kindler syndrome have a tendency to blister with minor trauma and are prone to sunburns. As individuals with Kindler syndrome age, they tend to have fewer problems with blistering and photosensitivity. However, pigment changes and thinning of the skin become more prominent.
抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』
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