Immunoglobulin-mediated membranoproliferative glomerulonephritis

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ORPHA:329903OMIM:615008N03.5
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Overview

Immunoglobulin-mediated membranoproliferative glomerulonephritis (Ig-MPGN) is a rare kidney disease in which the body's immune system causes damage to the tiny filtering units of the kidneys, called glomeruli. In this condition, immune proteins called immunoglobulins (antibodies) deposit in the kidney filters, triggering inflammation and thickening of the filtering membranes. This leads to progressive kidney damage over time. The disease can cause a range of symptoms including blood in the urine (which may appear pink, red, or cola-colored), protein leaking into the urine (causing foamy urine), swelling in the legs, ankles, or around the eyes, high blood pressure, and reduced kidney function. Some patients may also experience fatigue and general feelings of being unwell. The condition may be linked to underlying infections (such as hepatitis B or C), autoimmune diseases (like lupus), or other conditions that cause abnormal immune protein production. Treatment depends on the underlying cause and severity. It may include medications to suppress the immune system (such as corticosteroids, mycophenolate mofetil, or cyclophosphamide), blood pressure-lowering drugs (especially ACE inhibitors or ARBs to reduce protein loss), and treatment of any underlying condition driving the immune deposits. In some cases, the disease can progress to kidney failure requiring dialysis or kidney transplantation. Early diagnosis and treatment of the underlying cause can significantly improve outcomes.

Also known as:

Key symptoms:

Blood in the urine (pink, red, or dark-colored urine)Foamy or frothy urine from protein lossSwelling in the legs, ankles, feet, or around the eyesHigh blood pressureDecreased urine outputFatigue and tirednessUnexplained weight gain from fluid retentionLoss of appetiteNauseaShortness of breath from fluid buildupJoint pain (if related to autoimmune disease)Skin rash (if related to autoimmune disease)Headaches from high blood pressure

Inheritance

Multifactorial

Caused by a mix of several genes and environmental factors

Age of Onset

Variable

Can begin at different ages, from infancy through adulthood

Orphanet ↗OMIM ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for Immunoglobulin-mediated membranoproliferative glomerulonephritis.

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No actively recruiting trials found for Immunoglobulin-mediated membranoproliferative glomerulonephritis at this time.

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No specialists are currently listed for Immunoglobulin-mediated membranoproliferative glomerulonephritis.

View NORD Rare Disease Centers ↗Undiagnosed Disease Network ↗

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Immunoglobulin-mediated membranoproliferative glomerulonephritis.

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Community

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Latest news about Immunoglobulin-mediated membranoproliferative glomerulonephritis

2 articles
Clinical trialCLINICALTRIALSMar 26, 2026
New Clinical Trial: New Analytic Tools for aHUS and C3G Diagnosis (NCT05985122)
Researchers across 7 European countries are working together to develop better ways to diagnose two rare kidney diseases: atypical hemolytic-uremic syndrome (aH
Clinical trialCLINICALTRIALSMar 26, 2026
Trial Now Recruiting: Developing a Pipeline to Employ RNA-Seq as a Complementary Diagnostic Tool in Rare Diseases (NCT05996731)
Researchers are testing a new genetic tool called RNA-Seq to help diagnose rare diseases in children and adults whose current genetic tests came back negative.
See all news about Immunoglobulin-mediated membranoproliferative glomerulonephritis

Caregiver Resources

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Family & Caregiver Grants

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Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Questions for your doctor

Bring these to your next appointment

  • Q1.What is the underlying cause of my Ig-MPGN, and can it be treated?,How much kidney function have I lost, and what is my current kidney function level (GFR)?,What medications do you recommend, and what are their side effects?,How often will I need blood and urine tests to monitor my condition?,What dietary changes should I make to protect my kidneys?,What are the chances that my disease will progress to kidney failure, and what can we do to slow it down?,Should I be referred to any other specialists, and are there any clinical trials I might be eligible for?

Common questions about Immunoglobulin-mediated membranoproliferative glomerulonephritis

What is Immunoglobulin-mediated membranoproliferative glomerulonephritis?

Immunoglobulin-mediated membranoproliferative glomerulonephritis (Ig-MPGN) is a rare kidney disease in which the body's immune system causes damage to the tiny filtering units of the kidneys, called glomeruli. In this condition, immune proteins called immunoglobulins (antibodies) deposit in the kidney filters, triggering inflammation and thickening of the filtering membranes. This leads to progressive kidney damage over time. The disease can cause a range of symptoms including blood in the urine (which may appear pink, red, or cola-colored), protein leaking into the urine (causing foamy urine

How is Immunoglobulin-mediated membranoproliferative glomerulonephritis inherited?

Immunoglobulin-mediated membranoproliferative glomerulonephritis follows a multifactorial inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.