Autoimmune Thrombic Thrombocytopenia Purpura (commonly referred to as Immune Thrombocytopenia, or ITP) is a disease where blood does not clot due to lack of platelets or thrombocytes. Many with Autoimmune Thrombic Thrombocytopenia Purpura have larger, purple bruises called purpura and smaller bruises called petchiae which appear almost like a rash under the skin. For most individuals, Autoimmune Thrombic Thrombocytopenia Purpura is not a life-threatening disease and only lasts a few months. ITP is a fairly common blood disorder and may develop in children and adults. In most cases, ITP can be treated with medications, but in severe cases, removal of the spleen or transfusions, or may be necessary.
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Autoimmune Thrombotic Thrombocytopenic Purpura below!
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We have 233 products for the study of Autoimmune Thrombotic Thrombocytopenic Purpura that can be applied to Flow Cytometry, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.