Kindler syndrome: A very rare bullosa poikyloderma discovered in a baby

Abstract

Kindler syndrome is a very rare bullous dermatosis of the childhood. It is classified as a subtype of epidermolyse bullosa and is characterized by the occurrence of acral predisposing blisters, associated to poikyloderma, skin atrophy and photosensitivity. It may be sporadic or transmitted in an autosomic recessive model. The treatment is preventive and symptomatic. The aim of this article is to describe this syndrome, and explain its pathogeny via a case presentation with a literature review. *Correspondence to: Khadija Elboukhari, Departement of Dermatology, University Hospital of Fez, Morocco, E-mail: elboukharikhadija89@gmail.com