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Home Ankylosing SpondylitisStatistics
What is Ankylosing Spondylitis? Ankylosing Spondylitis is a form of arthritis that mainly involves the spine and joints of the extremities, such as the shoulders, hips and knees. Normal tissue that connects the vertebrae is gradually replaced by bone-like fibers, which fuse the spine and limit movement. It can also cause inflammation of the eyes, lungs, and heart It strikes primarily young men. When it does occur in females, it is harder to diagnose and the symptoms are often less severe. AS is a member of the family of diseases that attack the spine called spondylarthropathies, this group also includes Reiter's syndrome, some cases of psoriatic arthritis and the arthritis that accompanies inflammatory bowel disease. What causes it?Genetics appear to have a strong role in the cause of AS. All of the spondylarthropathies share a common genetic marker, called HLA-B27, which occurs in most affected individuals. What are the symptoms? The most common symptom of AS is low back pain and stiffness, the upper back and neck can also be involved. The shoulders, knees and hips may be swollen, stiff and painful. Fever, fatigue and weight loss are common. Eye inflammation and inflammation of the heart valves can occur in more severe cases. No one test can diagnose AS. Diagnosis is made based on medical history, physical exam, blood tests and x-rays. The HLA-B27 tissue antigen is present in 90% of patients compared to 5-8% incidence in general population. How is it treated? Treatment of AS is tailored to the individual. Each treatment plan usually consists of several different types of treatment. Scientists suspect that other genes are involved in AS. Genetic studies of families who have multiple members with AS are underway. The goal is to determine what genes influence disease onset, severity and distribution of symptoms. Some of the related information found on Arthritis Insight: For support visit our Chat Room and Message Boards. For more information: Spondyloarthropathy: by drdoc on-line
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