Nephrotic syndrome is a group of symptoms and abnormal test results that include protein in the urine, low blood protein levels in the blood, high cholesterol levels, high triglyceride levels, increased blood clot risk, and bodily swelling.

Nephrosis

Nephrotic syndrome is caused by different disorders that damage the kidneys. This damage leads to the release of too much protein in the urine.

The most common cause in children is minimal change disease. Membranous glomerulonephritis is the most common cause in adults. In both diseases, the glomeruli in the kidneys are damaged. Glomeruli are the structures that help filter wastes and fluids.

This condition can also occur due to:

• Cancer
• Diseases such as diabetes, systemic lupus erythematosus, multiple myeloma, and amyloidosis
• Genetic disorders
• Immune disorders
• Infections (such as strep throat, hepatitis, or mononucleosis)
• Use of certain medicines

It can occur with kidney disorders such as:

• Focal and segmental glomerulosclerosis
• Glomerulonephritis
• Mesangiocapillary glomerulonephritis

Nephrotic syndrome can affect all age groups. In children, it is most common between ages 2 and 6. This disorder occurs slightly more often in males than females.

Swelling (edema) is the most common symptom. It may occur:

• In the face and around the eyes (facial swelling)
• In the arms and legs, especially in the feet and ankles
• In the belly area (swollen abdomen)

Other symptoms include:

• Skin rash or sores
• Foamy appearance of the urine
• Poor appetite
• Weight gain (unintentional) from fluid retention
• Seizures

The goals of treatment are to relieve symptoms, prevent complications, and delay kidney damage. To control nephrotic syndrome, the disorder that is causing it must be treated. You may need treatment for life.

Treatments may include any of the following:

• Keeping blood pressure at or below 130/80 mm Hg to delay kidney damage. Angiotensin-converting enzyme (ACE) inhibitors or angiotensin receptor blockers (ARBs) are the medicines most often used. ACE inhibitors and ARBs may also help decrease the amount of protein lost in the urine.
• Corticosteroids and other medicines that suppress or quiet the immune system.
• Treating high cholesterol to reduce the risk for heart and blood vessel problems. A low-fat, low-cholesterol diet is usually not enough for people with nephrotic syndrome. Medicines to reduce cholesterol and triglycerides (usually statins) may be needed.
• A low-sodium diet may help with swelling in the hands and legs. Water pills (diuretics) may also help with this problem.
• Low-protein diets may be helpful. Your provider may suggest a moderate-protein diet (1 gram of protein per kilogram of body weight per day).
• Taking vitamin D supplements if nephrotic syndrome is long-term and is not responding to treatment.
• Taking blood thinner medicines to treat or prevent blood clots.

The outcome varies. Some people recover from the condition. Others develop long-term kidney disease and may eventually need dialysis and a kidney transplant.

Health problems that may result from nephrotic syndrome include:

• Acute kidney failure
• Hardening of the arteries and related heart diseases
• Chronic kidney disease
• Fluid overload, heart failure, fluid buildup in lungs
• Infections, including pneumococcal pneumonia
• Malnutrition
• Renal vein thrombosis

Contact your provider if:

• You or your child develops symptoms of nephrotic syndrome, including swelling in the face, belly, or arms and legs, or skin sores
• You or your child are being treated for nephrotic syndrome, but symptoms don't improve
• New symptoms develop, including cough, decreased urine output, discomfort with urination, fever, severe headache

Go to the emergency room or call the local emergency number (such as 911) if you have seizures.

Treating conditions that can cause nephrotic syndrome may help prevent the syndrome.

Published Date: September 02, 2025
Published By: Walead Latif, MD, Nephrologist and Clinical Associate Professor, Rutgers Medical School, Newark, NJ. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.

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Saha MK, Pendergraft WF, Jennette JC, Falk RJ. Primary glomerular disease. In: Yu ASL, Chertow GM, Luyckx VA, Marsden PA, Skorecki K, Taal MW, eds. Brenner and Rector's The Kidney. 11th ed. Philadelphia, PA: Elsevier; 2020:chap 31.