
Laboratory and clinical characteristics of patients diagnosed with HELLP syndrome due to microangiopathic hemolytic anemia and/or thrombocytopenia
Author(s) -
Ömer Ekinci,
Senar Ebinç
Publication year - 2020
Publication title -
van tıp dergisi (online)/van tıp dergisi
Language(s) - English
Resource type - Journals
eISSN - 2587-0351
pISSN - 1300-2694
DOI - 10.5505/vtd.2020.57984
Subject(s) - hellp syndrome , microangiopathic hemolytic anemia , medicine , schistocyte , hemolysis , anemia , pediatrics , preeclampsia , gastroenterology , platelet , pregnancy , thrombotic thrombocytopenic purpura , genetics , biology