
Moschcowitz Syndrome or Thrombotic Thrombocytopenic Purpura and Antiphospholipid Antibody Syndrome as a Rare Cause of Thrombocytopenia in Pregnancy Mimicking Hemolysis, Elevated Liver Enzymes, and Low Platelets Syndrome in a Patient with Bad Obstetric History: A Diagnostic Dilemma
Author(s) -
Anupama Bhute,
Sourya Acharya,
Neema Acharya,
Shazia Mohammad
Publication year - 2020
Publication title -
journal of south asian federation of obstetrics and gynaecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.108
H-Index - 8
eISSN - 0975-1920
pISSN - 0974-8938
DOI - 10.5005/jp-journals-10006-1791
Subject(s) - medicine , hellp syndrome , thrombotic thrombocytopenic purpura , thrombotic microangiopathy , antiphospholipid syndrome , microangiopathic hemolytic anemia , schistocyte , pregnancy , plasmapheresis , preeclampsia , hemolysis , hemolytic anemia , adamts13 , immunology , gastroenterology , platelet , antibody , disease , genetics , biology