Catastrophic antiphospholipid syndrome accompanied by complement regulatory gene mutation

Catastrophic antiphospholipid syndrome accompanied by complement regulatory gene mutation

Background. Antiphospholipid syndrome (APS), particularly the catastrophic antiphospholipid syndrome (CAPS), is one of the rare causes of thrombotic microangiopathy (TMA). CAPS is the most severe form of APS, especially when accompanied by complement dysregulation, causes progressive microvas...

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Bibliographic Details
Main Authors: Serim Pul, Betül Sözeri, Cemile Pehlivanoğlu, Deniz Filinte, Özde Nisa Türkkan, Mehtap Sak, Neslihan Çiçek, Serçin Güven, Ece Demirci Bodur, İbrahim Gökçe, Harika Alpay
Format: Article
Language:English
Published: Hacettepe University Institute of Child Health 2023-04-01
Series:The Turkish Journal of Pediatrics
Subjects:
antiphospholipid antibody syndrome
complement activation
human complement factor H-related protein
thrombotic microangiopathy
Online Access:https://turkjpediatr.org/article/view/39

Internet

https://turkjpediatr.org/article/view/39

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