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Topic: IgA nephropathy



  
 IgA nephropathy - Wikipedia, the free encyclopedia
Controlled trial of phenytoin therapy in IgA nephropathy.
A subset of IgA nephropathy patients, who have minimal change disease on light microscopy and clinically have nephrotic syndrome, show an exquisite response to steroids, behaving more or less like minimal change disease.
Fish oil therapy for IgA nephropathy: efficacy and interstudy variability.
http://en.wikipedia.org/wiki/IgA_nephritis   (2381 words)

  
 The International IGA Nephropathy Network
For the great majority of patients with IgA nephropathy only one person in the family is affected, so there is no need for the rest of the family to be checked.
We now know that the kidney problem in HSP is very similar to IgA nephropathy; but patients with HSP also get a skin rash and may have aches and pains in their joints and attacks of abdominal pain.
Further information for IgA nephropathy patients and their families can be found at the following websites.
http://www.igan-world.org/infopatients.htm   (2934 words)

  
 IgA Nephropathy
Further studies are needed to determine the long-term effectiveness and safety of this drug for the treatment of IgA Nephropathy.
However, if the drug is discontinued, most affected individuals will experience a relapse.
There may be associated pain in the loin area.
http://hw.healthdialog.com/kbase/nord/nord587.htm   (1136 words)

  
 IgA Nephropathy
Complete IgA nephropathy information from the patient's perspective, with medical...
Treatment of IgA Nephropathy in Children An evidence based approach
Post a question or comment on our Message Board
http://www.health-nexus.com/iga_nephropathy.htm   (286 words)

  
 The Foundation for IgA Nephropathy
We have no doctors or health professionals here, except some who might happen to be members of the email support group because they or a family member has IgA nephropathy.
The Foundation for IgA Nephropathy welcomes your feedback, suggestions or general questions about the website or administrative matters.
We do have many long-time IgAN patients though - which is what a peer support group is all about.
http://www.igan.ca   (849 words)

  
 Characteristics of Polymeric {lambda}-IgA Binding to Leukocytes in IgA Nephropathy -- Lai et al. 13 (9): 2309 -- ...
internalization of IgA (mIgA and pIgA) in granulocytes and monocytes.
affect the mesangial uptake of IgA in IgAN.
reflect rapid turnover and catabolism of IgA in the human body.
http://jasn.asnjournals.org/cgi/content/full/13/9/2309   (5518 words)

  
 IgA Nephropathy Support Network - Shedding Light on IgA Nephropathy
But before you can develop IgA Nephropathy, there must be some kind of trigger.
That makes it more difficult to attract governmental and private funding for research, to conduct trials of various treatments, and to link patients for mutual support.
Other treatments than prednisone, based on other rationales, have been tried with little or no success.
http://igansupport.org/faqs.html   (9588 words)

  
 Nephrology - IgA Nephropathy
There is no known effective treatment for IgA nephropathy.
Glomerulonephritis with a predominant pattern of IgA deposition occurs in other conditions including chronic hepatitis, SLE, and Henoch- Schonlein purpura.
This has prompted some to suggest that IgA nephropathy and HSP are illnesses along a continuum with a common etiology.
http://www.kidneydoctor.com/iga.htm   (527 words)

  
 What IgAN is (a summary)
IgAN patients who have a particularly "weakened immune system" may have it for other reasons than the IgAN.
People have considered allergies, things they may have been exposed to, foods, occupations, blood types, etc. So far, hundreds if not thousands have not been able to identify any such link.
It is not an autoimmune disease in the classic sense of that term, but it does involve the immune system.
http://www.igan.ca/id45.htm   (1165 words)

  
 IgA Nephropathy Home Page
If you have a medical condition that needs treatment it is generally considered a wise practice to seek professional help from medical practitioners when making choices as to treatment or care.
Our main purpose is to maintain this web site, collect data for research on the nature and possible treatments of the condition, and act to advocate a more thorough reading and understanding of this condition by patients and those in the medical world.
The IgAN Foundation's mission is to provide vital and the latest information on the diagnosis and treatment of IgA Nephropathy to patients, their families, and their healthcare providers.
http://www.iganfoundation.org   (1359 words)

  
 IgA Nephropathy
Cooperative treatment trials on the effectiveness of the drug prednisone are continuing in the United States.
The disease seems to cluster in certain families and in certain areas of the world.
The milder form of the disease seen after transplantation may be due to the use of anti-rejection drugs such as cyclosporine.
http://www.kidney.org/affiliate/NV/atoz/atozPrint.cfm?id=76   (730 words)

  
 UK NKF - Kidney Disease
This is not an easy condition to treat, and usually doctors rely on treatment of the blood pressure.
What's it really like - patient experiences of IgA Nephropathy
However, in some patients who have acute attacks after the 'flu, there may be some pain over the kidneys and a feeling of sickness for a couple of days.
http://www.kidney.org.uk/Medical-Info/kidney-disease/Iga.html   (735 words)

  
 Living Kidney Donor With IgA Nephropathy?
If the recipient did not have native-kidney IgA disease, such continued deposition is unlikely, the mesangium clears the old deposits, and the patient does well.

On the other hand, the third patient did not clear the deposits with time, though they did seem to decrease.

If the recipient has a disease that can present fairly often with "isolated hematuria" as defined above, the level of concern about microhematuria in the donor should probably rise considerably.
I would conclude from this that IgA nephropathy is a systemic disease, and that the prognosis for a patient who receives a kidney with a few IgA deposits depends heavily upon whether that person had IgA disease to begin with.
http://www.medscape.com/content/2002/00/44/38/443809/443809.xml   (1552 words)

  
 Immunoglobulin A (IgA) Nephropathy
IgA nephropathy is a very heterogeneous condition, which means that the presentation varies greatly between individuals and families.
Specific treatment for IgA nephropathy will be determined by your physician based on:
IgA nephropathy is a chronic kidney disease that may progress over a period of 10 to 20 years, and can lead to end-stage renal disease.
http://www.healthsystem.virginia.edu/uvahealth/adult_urology/iganeph.cfm   (446 words)

  
 IgA Nephropathy
This approach promises to provide an opportunity to develop rational therapies for IgA nephropathy.
Utilizing an experimental model of IgA immune complex-mediated nephropathy, our laboratory is focused on elucidating in vivo the cellular and molecular mechanisms that are associated with glomerular IgA immune deposits.
In addition, differential expression of extracellular matrix genes involved in the progressive stages of renal fibrosis is being characterized in a chronic model of this disease.
http://www.lifespan.org/Nephrology/research/patho.html   (126 words)

  
 Nephrology Nursing Journal: Primary IgA Nephropathy: Pathophysiology, Diagnosis, and Clinical Management.@ HighBeam ...
Nephrology Nursing Journal: Primary IgA Nephropathy: Pathophysiology, Diagnosis, and Clinical Management.@ HighBeam Research
Primary IgA Nephropathy: Pathophysiology, Diagnosis, and Clinical Management.
Search for more information on HighBeam Research for.
http://www.highbeam.com/library/doc0.asp?DOCID=1G1:74293613&refid=holomed_1   (216 words)

  
 Treatment of IgA Nephropathy with ACE Inhibitors: A Randomized and Controlled Trial -- Praga et al. 14 (6): 1578 -- ...
Blockade of the renin-angiotensin system increases graft survival in patients with chronic allograft nephropathy
IgA nephropathy treatment 25 years on: can we halt progression?
Treatment of IgA Nephropathy with ACE Inhibitors: A Randomized and Controlled Trial -- Praga et al.
http://jasn.asnjournals.org/cgi/content/abstract/14/6/1578   (536 words)

  
 NEJM -- IgA Nephropathy
Ng, R. Fish Oil Therapy in Recurrent IgA Nephropathy.
Steinmetz, O. M., Panzer, U., Harendza, S., Mertens, P. R., Ostendorf, T., Floege, J., Helmchen, U., Stahl, R. No association of the -2518 MCP-1 A/G promoter polymorphism with incidence and clinical course of IgA nephropathy.
Joseph P. Grande, M.D., Ph.D. IgA nephropathy is a relatively newly recognized disease, first
http://content.nejm.org/cgi/content/extract/347/10/738   (662 words)

  
 IgA Nephropathy
Information about clinics specializing in the treatment of IgA nephropathy
Experiences of family members of IgA nephropathy patients
Information about physicians specializing in the treatment of IgA nephropathy
http://aaaaq.com/kidney_urologic/IgA_nephropathy   (606 words)

  
 Disease - IgA nephropathy (Berger´s disease) - Detroit, Michigan
Risk factors include having a personal or family history of IgA nephropathy or Henoch Schonlein purpura (a form of vasculitis that affects many parts of the body, and may cause a kidney lesion that is identical to the lesion of Berger´s disease).
IgA nephropathy usually is discovered after one or more episodes of dark or bloody urine in a person with no other symptoms of kidney disorder.
Acute nephritic syndrome or nephrotic syndrome (groups of symptoms associated with decreased kidney functioning) may result.
http://www.henryfordhealth.org/14988.cfm   (538 words)

  
 Iga - IGA: Instituto Guatemalteco Americano
Information on IgA nephropathy as a medical condition with IgA nephropathy information including symptoms, diagnosis, misdiagnosis, treatment, prevention,
AllRefer Health - IgA Nephropathy (Berger's Disease) (Berger's
Detailed information on IgA nephropathy, including cause, symptoms, diagnosis, and treatment.
http://homefindout.com/?q=iga   (376 words)

  
 IgA nephropathy (Berger's disease) - MayoClinic.com
In rare cases, it can be associated with other conditions, such as Henoch-Schonlein purpura, severe liver disease and celiac disease.
IgA nephropathy is the most common form of glomerulonephritis.
Doctors may also refer to it as Berger's disease.
http://www.mayoclinic.com/health/bergers-disease/AN00887   (343 words)

  
 Applied Genetics News: GENOMICS: IgA Nephropathy Is Inherited
IgA nephropathy is thought to affect up to 1% of the population worldwide.
Lifton believes that it may yet turn out to regulate IgA metabolism in response to infection.
"Prior to this finding, IgA nephropathy was recognized as the most common form of glomerulonephritis worldwide, but its causes were unknown and were believed to be diverse," says Lifton.
http://www.findarticles.com/p/articles/mi_m0DED/is_4_21/ai_67541347   (477 words)

  
 IGA Nephropathy, The Transplant
Usually, IGA is caused by some kind of respiratory infection.
This is our story about our son, Darryl.
If you have been diagnosed with the disease of IGA Nephropathy or want to know our story, please continue to read our homepage, and we hope it is beneficial for you.
http://www.geocities.com/albertja_48446   (1405 words)

  
 IgA Nephropathy
Although IgA nephropathy is a primary renal disease, it is closely related to Schoenlein-Henoch purpura probably as a spectrum of a single disease the former being limited to the kidney and the latter occurring with a nonthrombopenic leukocytoclastic vasculitic purpura in association with arthalgias, and abdominal pain in addition to mesangial IgA deposits.
IgA nephropathy, also known as Berger disease or IgA/IgG Mesangial Nephropathy, is a glomerular disease with IgA-dominant or codominant (with IgG or IgM) mesangial immunoglobin deposits.
Tonsillectomy my reduce frequency of hematuric episodes (but may peri-operatively induce ARF)
http://www.med.unc.edu/medicine/web/iganephropathy.html   (654 words)

  
 IgA NEPHROPATHY ACCOMPANIED BY SILICA-DEPOSITED
The patient had glomerular injury due to IgA deposits, accompanied by interstitial damage due to silica deposition.
These granulomas were present both within the medulla and the cortex, however, crystals or crystal-bearing cells were not seen within the tubules.
A significant percentage of these patients had antinuclear antibodies, rheumatoid factor, immune complexes, and elevated IgG and IgA in their serum.
http://www.kfshrc.edu.sa/annals/191/98-177.html   (1118 words)

  
 Recurrent Renal Disease
Histopathological examination in recurrent IgA nephropathy most commonly shows increased mesangial matrix or mild mesangial proliferation.
Other patterns of glomerular injury include minimal change, endocapillary proliferation, membranous nephropathy and combined lesions.
Immunofluorescence examination and electron microscopy confirm the presence of IgA immune complex deposits in a mesangial location.
http://tpis.upmc.edu/tpis/kidney/KIgA.html   (70 words)

  
 Healthopedia.com - Berger's Disease (IgA Nephropathy, Berger's Nephropathy)
Berger's disease is generally believed to be an autoimmune disorder in which IgA antibodies interfere with normal kidney function.
Links to other sites are provided for information only -- they do not constitute endorsements of those other sites.
Antibodies are normally made by the immune system to fight infections.
http://www.healthopedia.com/bergers-disease   (473 words)

  
 IgA Nephropathy
Worldwide idiopathic IgA nephropathy is most common cause of chronic renal failure
Renal failure develops in ~30% of patients 5-25 years after diagnosis of idiopathic type
Likely has an immune component, antibody associated disease (B cell dysfunction)
http://www.outlinemed.com/demo/nephrol/11648.htm   (163 words)

  
 IgA Nephropathy
IgA nephropathy is a chronic kidney disease that usually first appears during adolescence and young adulthood and often progresses to kidney failure.
Healthwise disclaims any liability for the decisions you make based on this information.
Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
http://www.peacehealth.org/kbase/nord/nord587.htm   (346 words)

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