Pathology - Osler Weber Rendu Syndrome
Osler-Weber-Rendu Syndrome, also known as Hereditary Hemorrhagic Telangiectasia, is a medical condition. This is an autosomal dominant condition caused by mutations in TGF-Beta-binding proteins. It is more commonly observed among Utah Mormons. Study of diseases and their effects on the body. The epidermis and mucosal membranes of the oral cavity, respiratory system, gastrointestinal tract, and urinary tract experience localized widening and compression of small blood vessels called venules and capillaries. Symptoms and signs Recurrent bleeding from skin and mucous membrane wounds. Possible complications including gastrointestinal bleeding and nosebleeds. Laboratory results: Normocytic normochromic anemia refers to a type of anemia characterized by normal-sized red blood cells with normal hemoglobin content. Treatment options for epistaxis include nasal packing, cautery, and the use of estrogens to decrease bleeding. Sturge-Weber syndrome is a condition present at birth that is characterized by a birthmark on one side of the face, glaucoma, and abnormal growths on the membranes surrounding the brain. Clinically, it is evident through profound cognitive impairment, epileptic convulsions, and detachment of the retina.
0 Comments
Leave a Reply. |
Kembara XtraFacts about medicine and its subtopic such as anatomy, physiology, biochemistry, pharmacology, medicine, pediatrics, psychiatry, obstetrics and gynecology and surgery. Categories
All
|