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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...

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-д хадгалсан:
Номзүйн дэлгэрэнгүй
Үндсэн зохиолчид: Daria S. Fomina, Marina S. Lebedkina, Elena N. Bobrikova, Yulia D. Yukhnovskaya, Anna A. Roppelt, Olga A. Mukhina, Ulyana A. Markina, Yulia G. Alexeeva, Ekaterina A. Nikitina, Marcus Maurer, Alexander V. Karaulov, Maryana A. Lysenko, Thomas Buttgereit
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 нэмэх
Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!