HIGHLIGHTS
- who: Zsofia Polai from the Department of Internal Medicine and Haematology, Hungarian Angioedema Center of Reference and Excellence, Semmelweis have published the Article: C1-inhibitor/C1-inhibitor antibody complexes in acquired angioedema due to C1-inhibitor deficiency, in the Journal: (JOURNAL)
- what: Changes in CAC titers are suitable for monitoring C1-INH-AAE and the connecting underlying disease.
SUMMARY
Angioedema with C1-inhibitor (C1-INH) deficiency can be hereditary (C1-INH-HAE)-an autosomal dominant disorder caused by mutations in the SERPING1 gene- or acquired (C1-INH-AAE). Both are rare . . .
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