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Results 21 - 30 of 53 for Inherited thrombocytopenia
  1. Nakajo-Nishimura syndrome 
    ... a reduced amount of blood cells called platelets (thrombocytopenia), and abnormal deposits of calcium (calcification) in an ... function of these cells. PSMB8 This condition is inherited in an autosomal recessive pattern, which means both ...
    https://medlineplus.gov/genetics/condition/nakajo-nishimura-syndrome - Genetics
  2. Spondyloenchondrodysplasia with immune dysregulation 
    ... as a decrease in blood cells called platelets (thrombocytopenia), premature destruction of red blood cells (hemolytic anemia), ... disability, is currently unknown. ACP5 This condition is inherited in an autosomal recessive pattern, which means both ...
    https://medlineplus.gov/...hondrodysplasia-with-immune-dysregulation - Genetics
  3. Platelet Tests: MedlinePlus Medical Test 
    ... A lower-than-normal platelet count is called thrombocytopenia. This condition can cause you to bleed too ... results show a lower-than-normal platelet count (thrombocytopenia), it may be a sign of: A cancer ... marrow . Cirrhosis . Vitamin B12 deficiency (not enough). Gestational thrombocytopenia. A common, but mild, low-platelet condition that ...
    https://medlineplus.gov/lab-tests/platelet-tests - Medical Tests
  4. 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
  5. Thrombotic thrombocytopenic purpura 
    ... vessels. This leads to a low platelet count ( thrombocytopenia ). ... Complications may include: Kidney failure Low platelet count (thrombocytopenia) Low red blood cell count (caused by the ...
    https://medlineplus.gov/ency/article/000552.htm - Medical Encyclopedia
  6. About Antiphospholipid Syndrome (APS) From the National Institutes of Health (National Human Genome Research Institute)  
    Autoimmune Diseases/Specifics ... Autoimmune Diseases ... National Human Genome Research Institute ... From the National Institutes of Health ... Antiphospholipid Syndrome ...
    https://www.genome.gov/Genetic-Disorders/Antiphospholipid-Syndrome - External Health Links
  7. Learning about Gaucher Disease From the National Institutes of Health (National Human Genome Research Institute)  
    Gaucher disease is an autosomal recessive inherited disorder of metabolism where a type of fat (lipid) called glucocerebroside cannot be adequately degraded.
    https://www.genome.gov/Genetic-Disorders/Gaucher-Disease - External Health Links
  8. Pearson syndrome 
    ... numbers of white blood cells (neutropenia) and platelets (thrombocytopenia). Neutropenia can lead to frequent infections; thrombocytopenia sometimes causes easy bruising and bleeding. When visualized ...
    https://medlineplus.gov/genetics/condition/pearson-syndrome - Genetics
  9. Chromosome 1 
    ... chromosome 1 is involved in most cases of thrombocytopenia-absent radius (TAR) syndrome. TAR syndrome is characterized ... resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome. Am J Hum Genet. 2007 ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  10. Familial acute myeloid leukemia with mutated CEBPA 
    ... have a reduction in the amount of platelets (thrombocytopenia), which can result in easy bruising and abnormal ... gene that are passed down within families. These inherited mutations are present throughout a person's life ...
    https://medlineplus.gov/...acute-myeloid-leukemia-with-mutated-cebpa - Genetics
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