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Harris platelet syndrome (associated with giant platelet disorder) Macrothrombocytopenia and hearing loss; May–Hegglin anomaly (associated with giant platelet disorder) MYH9-related disease (associated with giant platelet disorder) PRKACG-related thrombocytopenia; Paris-Trousseau thrombocytopenia/Jacobsen syndrome; Sebastian syndrome; SLFN14 ...
Unlike ITP, the platelet count in gestational thrombocytopenia rarely goes below 100,000, and a platelet count below 80,000 is even more rare (seen in less than 0.1% of cases of gestational thrombocytopenia). Also unlike ITP, gestational thrombocytopenia is not a cause of neonatal or maternal bleeding, or neonatal thrombocytopenia. [63]
This characteristic is shared by two related syndromes, hemolytic-uremic syndrome (HUS) and atypical hemolytic uremic syndrome (aHUS). [4] Consequently, differential diagnosis of these TMA diseases is essential. Both TTP and HUS are characterized by fever, anemia, thrombocytopenia, renal failure, and neurological symptoms. Generally, TTP has ...
Diagnosis is done by the help of symptoms and only blood count abnormality is thrombocytopenia. [citation needed] Treatment. This section is empty.
Additionally, platelet antigen genotyping can be performed on the maternal and paternal blood to determine the exact nature of the incompatibility. [citation needed] Neonatal platelet counts on laboratory testing are typically under 20,000 μL −1. Higher counts may suggest a different diagnosis, such as maternal immune thrombocytopenic ...
Evans syndrome is an autoimmune disease in which an individual's immune system attacks their own red blood cells and platelets, the syndrome can include immune neutropenia. [ 1 ] [ 2 ] These immune cytopenias may occur simultaneously or sequentially.
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