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Target levels of functional C1-inhibitor in hereditary angioedema

✍ Scribed by C. E. Hack; A. Relan; E. S. van Amersfoort; M. Cicardi


Book ID
110887478
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
216 KB
Volume
67
Category
Article
ISSN
0105-4538

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Hereditary angioneurotic edema (HAE) is an autosomal dominant disorder characterized by episodic local subcutaneous and submucosal edema caused by the deficiency of activated C1 esterase inhibitor protein (C1-INH, type I (C1NH): reduced serum antigen level, type II: reduced activity and normal serum