Clinical evaluation of thrombotic microangiopathy: identification of patients with suspected atypical hemolytic uremic syndrome

Atypical hemolytic uremic syndrome (aHUS) is a rare genetic disorder caused by defective complement regulation resulting in thrombotic microangiopathy (TMA). Patients can present as children or adults. The syndrome consists of hemolytic anemia with schistocytosis, thrombocytopenia, significant renal...

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Detalles Bibliográficos
Autor principal: Shen, Yu-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5056489/
https://www.ncbi.nlm.nih.gov/pubmed/27766045
http://dx.doi.org/10.1186/s12959-016-0114-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5056489/
https://www.ncbi.nlm.nih.gov/pubmed/27766045
http://dx.doi.org/10.1186/s12959-016-0114-0

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