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Results 1 - 10 of 45 for Thrombocytopenia 1
  1. X-linked thrombocytopenia 
    ... cannot pass X-linked traits to their sons. Thrombocytopenia 1 XLT Genetic Testing Registry: Thrombocytopenia 1 X-linked thrombocytopenia with normal platelets National Organization ...
    https://medlineplus.gov/genetics/condition/x-linked-thrombocytopenia - Genetics
  2. Dyserythropoietic anemia and thrombocytopenia 
    ... linked traits to their sons. Dyserythropoietic anemia with thrombocytopenia GATA-1-related thrombocytopenia with dyserythropoiesis GATA1-related cytopenia GATA1- ...
    https://medlineplus.gov/...rythropoietic-anemia-and-thrombocytopenia - Genetics
  3. Thrombocytopenia-absent radius syndrome 
    ... to cow's milk that may worsen the thrombocytopenia associated with this disorder. TAR syndrome is a rare disorder, affecting fewer than 1 in 100,000 newborns. Mutations in the RBM8A ...
    https://medlineplus.gov/.../thrombocytopenia-absent-radius-syndrome - Genetics
  4. Chromosome 1 
    ... deletion in the 1q21.1 region of chromosome 1 is involved in most cases of thrombocytopenia-absent radius (TAR) syndrome. TAR syndrome is characterized ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  5. Immune thrombocytopenia 
    ... on PubMed Arnold DM. Bleeding complications in immune thrombocytopenia. Hematology Am Soc Hematol Educ Program. 2015;2015:237-42. doi: 10.1182/asheducation-2015.1.237. Citation on PubMed Doobaree IU, Nandigam R, ...
    https://medlineplus.gov/genetics/condition/immune-thrombocytopenia - Genetics
  6. 1q21.1 microdeletion 
    ... distinguish it from the genetic change that causes thrombocytopenia-absent radius syndrome (TAR syndrome). TAR syndrome results from the deletion of a different, smaller DNA segment in the chromosome 1q21.1 region near the area where the 1.35- ...
    https://medlineplus.gov/genetics/condition/1q211-microdeletion - Genetics
  7. STAT3 gene 
    ... on insulin-producing cells in the pancreas (type 1 diabetes), red blood cells (autoimmune hemolytic anemia), platelets (autoimmune thrombocytopenia), or tissues in the digestive tract (autoimmune enteropathy). ...
    https://medlineplus.gov/genetics/gene/stat3 - Genetics
  8. Wiskott-Aldrich syndrome 
    ... disease spectrum with two other disorders: X-linked thrombocytopenia and severe congenital neutropenia. These conditions have overlapping signs and symptoms and the same genetic cause. The estimated incidence of Wiskott-Aldrich syndrome is between 1 and 10 cases per million males worldwide; this ...
    https://medlineplus.gov/genetics/condition/wiskott-aldrich-syndrome - Genetics
  9. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome 
    ... low levels of red blood cells (anemia), platelets (thrombocytopenia), or certain white blood cells ... million people. Mutations in the ...
    https://medlineplus.gov/...ocrinopathy-enteropathy-x-linked-syndrome - Genetics
  10. Langerhans cell histiocytosis 
    ... clotting problems due to low numbers of platelets (thrombocytopenia).Other ... 1 in 50 affected individuals experience deterioration of neurological ...
    https://medlineplus.gov/.../condition/langerhans-cell-histiocytosis - Genetics
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