P51 Kindler synrome

• Published in: Archives of disease in childhood Vol. 102; no. Suppl 2; p. A54
• Main Authors: Dop, Dalia, Puiu, Ileana, Niculescu, Elena Carmen, Moro anu, Aritina Elvira, Stepan, Mioara Desdemona, Iano i, Simona
• Format: Journal Article
• Language: English
• Published: London BMJ Publishing Group LTD 01.06.2017
• Subjects: Biopsy; Constipation; Diagnosis; Epidermolysis bullosa; Extremities; Genetic Disorders; Hereditary diseases; Hyperpigmentation; Intellectual disabilities; Malignancy; Mucosa; Pediatrics; Photosensitivity; Stenosis

Kindler syndrome is a rare form of epidermolysis bullosa, which represents a group of hereditary diseases characterised by particular fragility of the skin and mucosa, manifesting in the appearance of bullae in minor traumas.We present the case of a 12-year-old girl who shows clinical elements chara...