With treatment, 90% of patients can expect symptom relief, and 75% go into complete remission
I was diagnosed with Wegener's Granulomatosis in March of 1971 (at age 21) I'm still alive and kicking in March 2012.
Wegener's granulomatosis is a very rare disease that affects many different organs and systems of the body.
because the tools were xtremely xpensive
There was a lack of technology.
Pangaea
Wegener's granulomatosis , now referred to as Granulomatosis with polyangiitis , is an inflammation of the blood vessels that feed the small and medium organs. Treatment involves long-term immunosuppression.
Wegener's granulomatosis, is one of a group of blood vessel disorders called vasculitis
I was diagnosed with Wegener's Granulomatosis in March of 1971 (at age 21) I'm still alive and kicking in March 2012.
At present, there are no preventive measures known for Wegener's granulomatosis.
Wegener's granulomatosis can cause Vasculitic neuropathy
Wegener's granulomatosis (WG) is not a contagious disease, and there is no evidence to suggest that it is hereditary either.
Wegener's granulomatosis is a very rare disease that affects many different organs and systems of the body.
No.
Yes.
why did other scientist not accpet Alfred Wegeners theory
no
Tuberculosis Endometriosis Sarcoidosis Amyloidosis Granulomatosis