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The C1 esterase inhibitor and hereditary angioedema

✍ Scribed by Michael M. Frank


Publisher
Springer
Year
1982
Tongue
English
Weight
397 KB
Volume
2
Category
Article
ISSN
0271-9142

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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