Nephrotic syndrome
Nephrotic Syndrome: Unraveling Symptoms, Causes, and Types
Symptoms:
Nephrotic syndrome is a kidney disorder characterized by a group of symptoms indicative of kidney damage. The primary symptoms include:
- Proteinuria: The hallmark of nephrotic syndrome is the presence of excessive protein in the urine. This occurs when the filtering units of the kidneys, known as glomeruli, become damaged. Healthy kidneys retain proteins, such as albumin, but in nephrotic syndrome, proteins leak into the urine, leading to foamy or frothy urine.
- Edema: Edema, or swelling, is a common manifestation. It typically occurs in the lower extremities, such as the legs, ankles, and feet, but can also affect the face. Edema results from the retention of fluid due to the kidneys’ reduced ability to regulate salt and water balance.
- Hypoalbuminemia: Nephrotic syndrome often leads to lower levels of albumin, a vital protein in the blood. Albumin plays a crucial role in maintaining blood volume and preventing fluid from leaking out of blood vessels. Reduced levels contribute to fluid accumulation in tissues, exacerbating edema.
- Hyperlipidemia: Elevated levels of lipids (fats) in the blood, including cholesterol and triglycerides, are commonly observed. The exact mechanisms leading to increased lipid levels are not fully understood, but it is a consistent feature of nephrotic syndrome.
Causes:
Nephrotic syndrome can have various underlying causes, and the specific cause may influence treatment and prognosis. Common causes include:
- Minimal Change Disease (MCD): Most prevalent in children, MCD is characterized by minimal changes visible under a microscope. The cause is often idiopathic, meaning it’s unknown. It responds well to treatment with corticosteroids.
- Focal Segmental Glomerulosclerosis (FSGS): This condition involves scarring in specific segments of the glomeruli, leading to protein leakage. FSGS can be primary, with an unknown cause, or secondary, resulting from genetic factors, infections, or other diseases.
- Membranous Nephropathy: Membranous nephropathy is characterized by thickening of the glomerular membranes, causing protein leakage. It can be secondary to conditions like autoimmune diseases, infections, or exposure to certain medications or toxins.
- Diabetic Nephropathy: A complication of diabetes, diabetic nephropathy occurs when persistent high blood sugar levels damage the glomeruli. Over time, this damage can lead to nephrotic syndrome.
- Systemic Lupus Erythematosus (SLE): Lupus is an autoimmune disease where the immune system attacks various organs, including the kidneys. Lupus nephritis can cause inflammation and contribute to nephrotic syndrome.
Types:
Nephrotic syndrome can be categorized into two main types based on its origin:
- Primary Nephrotic Syndrome:
– Characteristics: Occurs independently as a kidney disorder without an underlying cause.
– Common Causes: Minimal Change Disease (common in children), FSGS, and Membranous Nephropathy.
- Secondary Nephrotic Syndrome:
– Characteristics: Results from an underlying medical condition or disease affecting the kidneys.
– Common Causes: Diabetic Nephropathy, Lupus Nephritis, and certain infections.
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