C1q deficiency in activated PI3Kδ syndrome type 2.
Monogenic forms of vasculitis are rare, but increasingly recognised. Furthermore, genetic immunodeficiency is increasingly associated with inflammatory immune dysregulatory features, including vasculitis. We describe a child of non-consanguineous parents who presented with chronic digital vasculitis...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2019-11-01
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| Series: | Frontiers in Immunology |
| Subjects: | |
| Online Access: | http://journal.frontiersin.org/Journal/10.3389/fimmu.2019.02589/full |