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Results 1 - 8 of 8 for Thrombocytopenia 6
  1. NBEAL2 gene 
    ... phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and alpha-granule deficiency. Haematologica. 2013 Jun;98(6):868-74. doi: 10.3324/haematol.2012.075861. ...
    https://medlineplus.gov/genetics/gene/nbeal2 - Genetics
  2. GP1BA gene 
    ... clotting. More About This Health Condition ... blood (thrombocytopenia) and mild bleeding abnormalities. In contrast to mutations ...
    https://medlineplus.gov/genetics/gene/gp1ba - Genetics
  3. WAS gene 
    ... gene have been found to cause X-linked thrombocytopenia, a blood disorder characterized by a decrease in ... the actin cytoskeleton. In people with X-linked thrombocytopenia, these signaling problems primarily affect the development of ...
    https://medlineplus.gov/genetics/gene/was - Genetics
  4. GNE gene 
    ... found to have a lower number of platelets (thrombocytopenia), a condition called GNE-related thrombocytopenia. When variants in the GNE gene reduce the ...
    https://medlineplus.gov/genetics/gene/gne - Genetics
  5. MPL gene 
    ... gene cause a rare condition called congenital amegakaryocytic thrombocytopenia (CAMT). This condition begins in infancy and is ... by low numbers of megakaryocytes (megakaryocytopenia) and platelets (thrombocytopenia). CAMT can lead to an impairment of bone ...
    https://medlineplus.gov/genetics/gene/mpl - Genetics
  6. STAT3 gene 
    ... red blood cells (autoimmune hemolytic anemia), platelets (autoimmune thrombocytopenia), or tissues in the digestive tract (autoimmune enteropathy). ... Hurt EM, Farrar WL. The role of IL-6 and STAT3 in inflammation and cancer. Eur J ...
    https://medlineplus.gov/genetics/gene/stat3 - Genetics
  7. STIM1 gene 
    ... a low number of blood cells called platelets (thrombocytopenia) and consequent bleeding problems, a muscle disorder called ... to break down earlier than usual, leading to thrombocytopenia and bleeding problems in people with Stormorken syndrome. ...
    https://medlineplus.gov/genetics/gene/stim1 - Genetics
  8. ITGB3 gene 
    ... L718P mutation in a pedigree with autosomal dominant thrombocytopenia with anisocytosis. Br J Haematol. 2013 Feb;160( ... alphaIIbbeta3 integrin. Semin Thromb Hemost. 2011 Sep;37(6):698-706. doi: 10.1055/s-0031-1291380. ...
    https://medlineplus.gov/genetics/gene/itgb3 - Genetics