Focal Segmental Glomerulosclerosis (FSGS)

Focal segmental glomerulosclerosis (FSGS) is a disease in which scar tissue develops on the parts of the kidneys that filter waste from the blood (glomeruli). This condition can lead to kidney failure if left untreated.

Causes and Risk Factors

The exact cause of FSGS is not fully understood, but it is believed to be related to a combination of genetic and environmental factors. Some possible causes include:

Symptoms

The symptoms of FSGS can vary depending on the severity of the condition. Common symptoms include:

Diagnosis

FSGS is typically diagnosed through a combination of physical examination, medical history, laboratory tests, and kidney biopsy. The following tests may be used:

Treatment

The treatment of FSGS depends on the underlying cause and severity of the condition. The following treatments may be used:

  • Medications to control blood pressure, reduce proteinuria, and slow disease progression
  • Corticosteroids or immunosuppressive medications to reduce inflammation and immune system activity
  • Diuretics to manage edema and fluid retention
  • Lifestyle modifications such as a low-sodium diet, weight loss, and regular exercise
  • Kidney transplantation in cases of end-stage renal disease

Prognosis

The prognosis for FSGS varies depending on the severity of the condition and response to treatment. With proper management, some patients may experience remission or stabilization of their kidney function, while others may progress to end-stage renal disease requiring dialysis or transplantation.

Frequently Asked Questions (FAQs)

What is Focal Segmental Glomerulosclerosis (FSGS)?
A disease in which scar tissue develops on the parts of the kidneys that filter waste from the blood.

What are the symptoms of FSGS?
May include proteinuria, hematuria, hypertension, and edema, although some cases may be asymptomatic.

What causes FSGS?
The exact cause is often unknown, but it can be related to genetic factors, infections, or secondary to other conditions.

Is FSGS inherited?
Some cases of FSGS appear to be inherited, while others are sporadic or secondary to another condition.

How is FSGS diagnosed?
Typically through a combination of urine tests, blood tests, and kidney biopsy.

Can FSGS be treated?
Treatment options may include medications to reduce proteinuria and slow disease progression, but the effectiveness can vary.

What are the complications of FSGS?
May include end-stage renal disease, nephrotic syndrome, and increased risk of cardiovascular disease.

Is there a cure for FSGS?
There is no known cure, but treatment can help manage symptoms and slow disease progression in some cases.

Can lifestyle changes help manage FSGS?
Possibly, as controlling blood pressure, reducing protein intake, and maintaining a healthy weight may help slow disease progression.

What is the prognosis for someone with FSGS?
The outlook varies widely depending on the underlying cause, severity of symptoms, and response to treatment.

Article last updated on: 18th October 2025.
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