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780 Possible Causes for Hemophilia B

  • Hemophilia B

    There are different types of hemophilia: A, B and Von Willebrand disease. Hemophilia B is the second most common type of hemophilia.[] B What are the Risk Factors for Hemophilia B?[] , or following surgery or tooth extraction (severe hemophilia B; see this term).[]

  • Sickle Cell Thalassemia Disease

    B.[] […] achieve high efficiency transduction of HSCs, given the proven safety and efficacy of AAV vectors in clinical trials in gene therapy of Leber’s congenital amaurosis and hemophilia[]

  • Hemophilia A

    Hemophilia A and Hemophilia B are two types of Hemophilia.[] A/hemophilia B and ACS.[] Type B hemophilia is caused by a deficiency of factor IX.[]

  • Dyschromatosis Universalis Hereditaria 1

    This is now known to have been Hemophilia B, Hemophilia B, also known as Christmas Disease, a blood clotting disorder caused by a mutation of the Factor IX gene and leading[] It is rarer than hemophilia A, as noted above, it was common among the descendants of Queen Victoria.[]

  • Chronic Liver Disease

    Univariate and multivariate logistic regression (MLR) analyses were performed.A total of 532 PWH were included with either hemophilia A (n   467) or hemophilia B (n   65).[] Hepatitis C virus (HCV), human immunodeficiency virus (HIV), total cholesterol, and severe hemophilia were significant risk factors in univariate logistic regressions.[]

  • Ectodermal Dysplasia with Natal Teeth Type Turnpenny

    Hemophilia A Hemophilia B Mild hemophilia A Mild hemophilia B Moderately severe hemophilia A Moderately severe hemophilia B Rare hemorrhagic disorder due to a constitutional[] hemophilia B Symptomatic form of hemophilia A in female carriers Symptomatic form of hemophilia B in female carriers Von Willebrand disease[] […] platelet anomaly Rare hemorrhagic disorder due to a constitutional thrombocytopenia Rare hemorrhagic disorder due to a qualitative platelet defect Severe hemophilia A Severe[]

  • Hypoplastic Right Heart Syndrome

    I also carry a bleeding disorder gene for hemophilia b, which has a 50% chance of him having the disorder.[]

  • Ornithine Transcarbamylase Deficiency

    “We are pleased to have received U.S. orphan designation for two of our lead candidates, DTX101 for hemophilia B and now DTX301, recognizing the substantial need for new approaches[] […] to hemophilia and inborn errors of metabolism,” said Annalisa Jenkins, MBBS, MRCP, CEO of Dimension.[]

  • Galactosialidosis

    B; 3) implemented a GMP compliant production and purification methodology for the hPPCA vector that we anticipate using in our clinical trial; and 4) defined with the FDA[] (PPCA ) mouse model; 2) demonstrated that an analogous rAAV vector encoding human coagulation Factor IX restores FIX production in participants in a clinical trial with hemophilia[]

  • Factor IX

    At a Glance Hemophilia B, a deficiency of factor IX, is clinically indistinguishable from hemophilia A, a deficiency of factor VIII.[] RESULTS: All 18 children had severe hemophilia B, and in each an inhibitor antibody to FIX developed.[] PubMed Search: Factor IX deficiency[title] AND Hemophilia B [title] Cite this page: Factor IX deficiency (hemophilia B) . website. .[]

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