Recurrent angioedema manifestation and treatment response in two patients from different families caring the myoferlin gene mutation: case series
Abstract Data on hereditary angioedema with normal C1 inhibitor levels are currently limited. To date, only one Italian family with HAE-MYOF has been described, comprising exclusively female members. The angioedema (AE) of head and neck area with the teenage onset, triggered by menses and high fever...
-д хадгалсан:
| Үндсэн зохиолчид: | , , , , , , , , , , , , |
|---|---|
| Формат: | Artigo |
| Хэл сонгох: | Inglês |
| Хэвлэсэн: |
BMC
2025-08-01
|
| Цуврал: | Orphanet Journal of Rare Diseases |
| Нөхцлүүд: | |
| Онлайн хандалт: | https://doi.org/10.1186/s13023-025-03932-9 |
| Шошгууд: |
Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!
|
