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Hereditary "angioedema," type II
- ... INH in the blood. The variants that cause hereditary angioedema due to C1-INH deficiency type II usually occur in a specific region of the gene called exon 8. These variants lead to the production of a C1-INH that ... with hereditary angioedema due to C1-INH deficiency. More About This ...
- ... deficiency and hereditary angioedema with normal C1-INH. Hereditary angioedema due to C1-INH deficiency is further divided into two types: type I occurs when C1-INH levels are low, and type II occurs when the C1-INH protein is not ...
- ... and sacubitril is also used to treat certain types of heart failure in children 1 ... called neprilysin inhibitors. It works to help control blood volume.