Clinical case of recurrent aHUS after allogeneic cadaveric kidney transplantation

Introduction. Atypical hemolytic uremic syndrome (aHUS) is a systemic orphan disease that reproduces as an uncontrolled activation of the alternative pathway of the complement system and is expressed as systemic thrombotic microangiopathy (TMA). The classical triad of aHUS symptoms are hemolytic ane...

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Hlavní autoři:	S. V. Popov, A. M. Esayan, R. G. Guseynov, I. N. Orlov, E. V. Lomonosova, V. V. Perepelitsa, О. A. Vorobyeva, A. V. Sadovnikova, T. A. Lelyavina
Médium:	Artigo
Jazyk:	Russo
Vydáno:	Federal Research Center of Transplantology and Artificial Organs named after V.I.Shumakov 2024-01-01
Edice:	Вестник трансплантологии и искусственных органов
Témata:	atypical hemolytic uremic syndrome thrombotic microangiopathy kidney transplantation eculizumab hemolytic anemia thrombocytopenia
On-line přístup:	https://journal.transpl.ru/vtio/article/view/1641
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