National Institutes of Health
- The primary NIH organization for research on Wegener's Granulomatosis is the National Institute of Allergy and Infectious Diseases
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National Institutes of Health
Wegener's Granulomatosis
Wegener's granulomatosis is a rare disease. It is a type of vasculitis, or inflammation of the blood vessels. This limits the flow of blood to important organs, causing damage. It can affect any organ, but it mainly affects the sinuses, nose, trachea (windpipe), lungs and kidneys.
The cause of Wegener's granulomatosis is unknown. Symptoms may include joint pain, weakness, tiredness and cold symptoms such as a runny nose that doesn't get better. Doctors use blood tests and chest x-rays to diagnose the disease and rule out other causes of the symptoms.
Early treatment is important. Most people improve with medicines to slow or stop the inflammation.
NIH: National Institute of Allergy and Infectious Diseases
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Wegener's Granulomatosis(National Institute of Allergy and Infectious Diseases)
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Wegener's Granulomatosis
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Overviews
- Granulomatosis with Polyangiitis (Wegener's)(American College of Rheumatology)
- Wegener's Granulomatosis(Johns Hopkins Vasculitis Center)
- Wegener's Granulomatosis(Mayo Foundation for Medical Education and Research)
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Diagnosis/Symptoms
- ANCA / MPO / PR3 Antibodies(American Association for Clinical Chemistry)
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Treatment
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Wegener's Granulomatosis: Treatment(National Institute of Arthritis and Musculoskeletal and Skin Diseases)
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Wegener's Granulomatosis: Treatment
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Related Issues
- Remission and Flares(Vasculitis Foundation)
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Clinical Trials
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ClinicalTrials.gov: Wegener Granulomatosis(National Institutes of Health)
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ClinicalTrials.gov: Wegener Granulomatosis
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Journal Articles
References and abstracts from MEDLINE/PubMed (National Library of Medicine)
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Organizations
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Patient Handouts
- Wegener's granulomatosis
- Also available in Spanish
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