... Millikan PD, Balamohan SM, Raskind WH, Kacena MA. Inherited thrombocytopenia due to GATA-1 mutations. Semin Thromb Hemost. ...

... acquired form of thrombotic thrombocytopenic purpura is not inherited. Chronic relapsing thrombotic thrombocytopenic purpura Familial thrombotic thrombocytopenia purpura Moschkowitz disease Purpura, thrombotic thrombocytopenic TTP Genetic ...

... they do not appear to be caused by inherited gene mutations. These acquired cases of glycoprotein VI deficiency are associated with autoimmune disorders such as immune thrombocytopenia purpura, Graves' disease, or systemic lupus erythematosus (SLE). ...

... red blood cells (autoimmune hemolytic anemia), platelets (autoimmune thrombocytopenia), or tissues in the digestive tract (autoimmune enteropathy). The mutations involved in these conditions are typically inherited and are found in every cell of the ...

Thrombocytopenia-absent radius (TAR) syndrome is characterized by the absence of a bone called the radius in each forearm and a shortage (deficiency) of blood cells involved ...

... same genetic cause, Wiskott-Aldrich syndrome, X-linked thrombocytopenia, and severe congenital neutropenia are sometimes collectively referred to as WAS-related disorders. WAS This condition is inherited in an X-linked pattern. A condition is ...

... to break down earlier than usual, leading to thrombocytopenia and bleeding problems in people with Stormorken syndrome. It is unknown how constitutively active STIM1 leads to the other features of the disorder. STIM1 This condition is inherited in an autosomal dominant pattern, which means one ...

... disorder 11q- deletion syndrome 11q23 deletion disorder Jacobsen thrombocytopenia Genetic Testing Registry: 11q partial monosomy syndrome Jacobsen ...

... acquired von Willebrand syndrome, is not caused by inherited gene variants (also called mutations). Acquired von Willebrand ... 1 and type 2 von Willebrand disease are inherited in an autosomal dominant pattern, which means one ...