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Correspondence response
Response to: ’A20 haploinsufficiency (HA20): clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease' by Aeschlimann et al
  1. Florence A Aeschlimann1,2,
  2. Ronald M Laxer1,2,3
  1. 1Division of Rheumatology, The Hospital for Sick Children, Toronto, Ontario, Canada
  2. 2Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada
  3. 3Department of Medicine, University of Toronto, Toronto, Ontario, Canada
  1. Correspondence to Dr Florence A Aeschlimann, Division of Rheumatology, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada; florence.aeschlimann{at}aphp.fr

http://dx.doi.org/10.1136/annrheumdis-2018-213359

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We thank Dr Berteau et al1 for sharing their experience of a family diagnosed with HA20 based on a Behçet-like disease phenotype and an autosomal-dominant inheritance pattern.

The presentation and disease course described in the mother and her two children support the findings described in our cohort2 and in a recent large cohort of Japanese patients with HA20.3 An interesting …

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