Camptodactlyly in Pediatric Practice: Blau Syndrome - 20/05/20
Doi : 10.1016/j.jpeds.2020.01.057
Julie Poline, MD
Department of General Pediatrics, Paediatric Internal Medicine, Rheumatology and Infectious Diseases, National Reference Centre for Rare Paediatric Inflammatory Rheumatisms and Systemic Auto-immune diseases RAISE, Robert Debré University Hospital, Assistance Publique-Hôpitaux de Paris
Université Paris Diderot-Sorbonne Paris-Cité, INSERM, UMR1149
Biology and Genetics of Bacterial Cell Wall Unit, Pasteur Institute, Paris, France
Emmanuelle Bourrat, MD ∗
Department of General Pediatrics, Paediatric Internal Medicine, Rheumatology and Infectious Diseases, National Reference Centre for Rare Paediatric Inflammatory Rheumatisms and Systemic Auto-immune diseases RAISE, Robert Debré University Hospital, Assistance Publique-Hôpitaux de Paris
Department of Dermatology, Saint Louis University Hospital, Assistance Publique-Hôpitaux de Paris
Ulrich Meinzer, MD, PhD ∗
Department of General Pediatrics, Paediatric Internal Medicine, Rheumatology and Infectious Diseases, National Reference Centre for Rare Paediatric Inflammatory Rheumatisms and Systemic Auto-immune diseases RAISE, Robert Debré University Hospital, Assistance Publique-Hôpitaux de Paris
Université Paris Diderot-Sorbonne Paris-Cité, INSERM, UMR1149
Biology and Genetics of Bacterial Cell Wall Unit, Pasteur Institute, Paris, France
Keywords : Blau syndrome, camptodactyly, autoinflammatory disease, granuloma, pediatric, sarcoidosis, NOD2, millimetric papules
© 2020
Elsevier Inc. Tous droits réservés.
Vol 221
P. 257-259 - juin 2020 Retour au numéro
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