Nephrology Dialysis Transplantation · 2010 · 67 citations · 23 references
MedicineCardiologyHematologyHuman GeneticsMedical GeneticsPathophysiologyAcute Coronary SyndromesCardiovascular DiseaseCardiovascular PathologyCoronary Artery DiseaseHemostatic DisordersThrombosisCardiac Causes Of DeathCardiovascular Risk Factor ManagementEarly Cardiovascular Risk Factor IdentificationMutationMyocardial Infarction GeneticsSudden Cardiac Death PredispositionThrombosis In Hemolytic Disorders
Cardiac complications are frequently seen in thrombotic thrombocytopaenic purpura related to ADAMTS13 deficiency. We describe the case of a 43-year-old woman who was diagnosed with an atypical haemolytic-uraemic syndrome (aHUS) associated with a pathogenic mutation in the factor H gene (C623S). After 15 days of treatment, she suffered a sudden cardiac arrest and died despite intensive resuscitation attempts. She showed only one cardiovascular risk factor, hypercholesterolaemia. Her sudden death was secondary to cardiac infarction related to a coronary thrombotic microangiopathy. This is the first case of aHUS related to a mutation in the factor H gene associated with cardiac microangiopathy. This case emphasizes the need to screen for cardiac complication during the treatment of aHUS.
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Thrombomodulin Mutations in Atypical Hemolytic–Uremic Syndrome
Mieke Delvaeye, Marina Noris, Astrid De Vriese et al. · New England Journal of Medicine · 2009 · 546 citations · Full text
Medicine, Genetics, Hematology +15
Elena Goicoechea de Jorge, Claire L. Harris, Jorge Esparza-Gordillo et al. · Proceedings of the National Academy of Sciences · 2006 · 445 citations · Full text