RECOMMENDATION 3 |
We recommend that patients who are suspected to have HAE and have normal C1–INH levels and function are assessed for known mutations underlying HAE-nC1-INH. |
91% agreement, evidence level D |
RECOMMENDATION 3 |
We recommend that patients who are suspected to have HAE and have normal C1–INH levels and function are assessed for known mutations underlying HAE-nC1-INH. |
91% agreement, evidence level D |