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The Kindler syndrome, the fourth major type of hereditary epidermolysis bullosa (HEB), is a rare autosomal recessive genodermatoses, characterized by trauma-induced blistering, cutaneous atrophy, and progressive poikiloderma, in association with mucosal inflammation. We report tow  new sibling cases of this rare syndrome.

Kindler Syndrome : Clinical Particularities about Two Cases Reports in Two Siblings