Hereditary Angioedema (HAE) is often unrecognized or misdiagnosed because it is so rare, and because its symptoms are similar to many other, more common conditions. People who have HAE have often been misdiagnosed with:
The lack of an accurate diagnosis can have serious consequences. Patients with undiagnosed HAE may undergo unnecessary medical procedures (e.g., appendectomy, exploratory laparotomy), or receive ineffective treatments.
Because HAE is usually passed down from parent to child, your family history is an important diagnostic tool for your doctor. However, some patients with hereditary angioedema did not receive the defective gene involved in HAE from a parent; rather, the gene mutated on its own. In some cases, this can lead to a delayed diagnosis.
If your doctor suspects that you have HAE, he or she will conduct blood tests, which will confirm your diagnosis. With HAE, laboratory results show:
If you suffer from unexplained swelling or other HAE symptoms, ask your doctor about getting tested for the disease.
To start the conversation about hereditary angioedema, complete the “Do I Have HAE?” questionnaire and share the results with your doctor.
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