Abstract
For patients with the rare immunological syndrome acquired angioedema associated with C1 inhibitor deficiency, replacement therapy with plasma-derived C1 INH concentrate is standard treatment. For those who develop resistance to replacement therapy, another drug has been shown to be successful in managing acute episodes.
Original language | English |
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Pages (from-to) | 50-51 |
Number of pages | 2 |
Journal | Medicine Today |
Volume | 16 |
Issue number | 1 |
Publication status | Published - 2015 |
Keywords
- angioneurotic edema