Aplasia cutis congenita with dystrophic epidermolysis bullosa: clinical and mutational study

Author:

Chiaverini C.12,Charlesworth A.12,Fernandez A.1,Barbarot S.3,Bessis D.4,Bodemer C.5,Bursztejn A.-C.6,Cobo A.-M.7,Del Rio M.8,D'Incan M.9,Labrèze C.10,Langlet C.11,Mazereeuw J.12,Miquel J.13,Vabres P.14,Meneguzzi G.2,Lacour J.-P.12

Affiliation:

1. French Reference Centre for Inherited Epidermolysis Bullosa; Archet Hospital; BP 3079 06202 NICE Cedex3 France

2. INSERM U1081, CNRS UMR7284; Institute for Research on Cancer and Aging, Nice (IRCAN); University of Nice Sophia Antipolis, Faculty of Medicine; 28 Avenue Valombrose F-06107 Nice France

3. Competence Centre for Rare Skin Diseases; Department of Dermatology; CHU Nantes; Nantes France

4. Department of Dermatology; Saint Eloi Hospital; Montpellier France

5. French Reference Centre for Genetic Skin Disorders (MAGEC); CHU Necker for Sick Children; University-Paris Descartes; Institute Imagine; APHP; Paris France

6. Department of Dermatology; Fournier Hospital; Nancy France

7. Department of Genetics; Donostia Hospital; San Sebastian Spain

8. Regenerative Medicine Unit; Department of Bioengineering; CIEMAT and CIBER on Rare Diseases; Universidad Carlos III; Madrid Spain

9. Department of Dermatology; Estaing Hospital; Clermont-Ferrand France

10. National Centre for Rare Skin Disorders and Diseases; Pellegrin Enfants Hospital; Bordeaux France

11. Department of Pediatrics 2; Hautepierre Hospital; Strasbourg France

12. Reference Centre for Rare Skin Diseases; Department of Dermatology; Larrey Hospital; Toulouse France

13. Department of Dermatology; Pontchaillou Hospital; Rennes France

14. Department of Dermatology; Bocage Hospital; Dijon France

Publisher

Wiley

Subject

Dermatology

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