Indian Journal of Dermatology
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CASE REPORT
Year : 2010  |  Volume : 55  |  Issue : 4  |  Page : 393-396

Kindler's syndrome: A case series of three Indian children


1 Department of Dermatology, Venereology, and Leprosy, R.G.Kar Medical College, Kolkata, India
2 Department of Dermatology, School of Tropical Medicine, Kolkata, India

Correspondence Address:
Sudip Kumar Ghosh
Vill. and P.O-Rajballavpur (via-Maslandpur), District - 24 Parganas (North) - 743289, West Bengal
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0019-5154.74568

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Kindler's syndrome is a very rare genodermatosis characterized by acral blistering starting in infancy, photosensitivity, progressive poikiloderma, cutaneous atrophy, and various forms of mucosal involvement. A large number of other cutaneous and extracutaneous features have also been described. We report here three cases of Kindler's syndrome from eastern India for the rarity of the syndrome and to emphasize the importance of considering this condition in the differential diagnosis of disorders that can cause blistering, cutaneous atrophy, and/or poikilodermatous skin changes.


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