hereditary hemorrhagic telangiectasia การใช้

• A major research interest has been the disease, hereditary hemorrhagic telangiectasia.
• House wakes up and correctly diagnoses the patient with hereditary hemorrhagic telangiectasia, surprising the team.
• Mutations in GDF2 have been identified in patients with a vascular disorder phenotypically overlapping with hereditary hemorrhagic telangiectasia.
• OWR is a legitamite abbreviation for Osler-Weber-Rendu Syndrome which is also known as Hereditary hemorrhagic telangiectasia.
• In humans endoglin may be involved in the autosomal dominant disorder known as hereditary hemorrhagic telangiectasia ( HHT ) type 1.
• Mutations in ALK1 and endoglin cause hereditary hemorrhagic telangiectasia ( HHT ), a rare but life-threatening genetic disorder that leads to abnormal blood vessel formation in multiple tissues and organs of the body.
• Non-infectious diseases that may result in symptoms similar to those of EVD include acute promyelocytic leukemia, hemolytic uremic syndrome, snake envenomation, clotting factor deficiencies / platelet disorders, thrombotic thrombocytopenic purpura, hereditary hemorrhagic telangiectasia, Kawasaki disease, and warfarin poisoning.