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IgA nephropathy is the most common type of glomerulonephritis in adults worldwide.
But, since IgA nephropathy may run in families, genetic factors probably contribute to the disease.
The changes are indistinguishable from those observed in IgA nephropathy.
He was given a diagnosis of IgA nephropathy, a disease that can lead to kidney failure.
Patients with IgA nephropathy often have high cholesterol.
There are a few additional caveats that have to be considered while treating IgA nephropathy.
The role of fish oil/omega-3 fatty acids in the treatment of IgA nephropathy.
There is also a striking geographic variation in the prevalence of IgA nephropathy throughout the world.
For preserving kidney function in patients with severe IgA nephropathy: 4-8 grams/day of fish oil has been used.
While not dangerous in itself, it maybe a symptom of kidney disease, such as IgA nephropathy, which should be monitored by a doctor.
The long-term outcome of patients with IgA nephropathy treated with fish oil in a controlled trial.
Reducing cholesterol - through diet, medication, or both - appears to help slow the progression of IgA nephropathy.
In IgA nephropathy, episodes of frank hematuria are more common, and a family history is less common.
Important It is possible that the main title of the report IgA Nephropathy is not the name you expected.
IgA nephropathy is caused by IgA deposits in the kidneys.
Again, IgA nephropathy also remains undiagnosed.
HSP is associated with a more benign prognosis than IgA nephropathy.
In children and younger adults, the history and association with respiratory infection can raise the suspicion of IgA nephropathy.
Nevertheless, IgA nephropathy, which was initially thought to be a benign disease, has been shown to have not-so-benign long term outcomes.
Not to be confused with Berger's disease (IgA nephropathy)
A randomized trial of high-dose compared with low-dose omega-3 fatty acids in severe IgA nephropathy.
Publication: IgA Nephropathy.
Diagnosis of IgA Nephropathy and a search for any associated disease occasionally reveals such an underlying serious systemic disease.
Histologically, IgA nephropathy may show mesangial widening and focal and segmental inflammation.
IgA nephropathy has a very variable course, ranging from a benign recurrent hematuria up to a rapid progression to chronic renal failure.