Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis digital illustration

Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis Save


ICD-10 code: N07.5

Disease category: N07: Hereditary nephropathy, not elsewhere classified

Understanding Hereditary Nephropathy with Diffuse Mesangiocapillary Glomerulonephritis

Hereditary Nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis, is a rare genetic disorder that affects the kidneys. The condition is caused by mutations in certain genes that are responsible for the production of proteins that are essential for the proper functioning of the kidneys.

Diffuse Mesangiocapillary Glomerulonephritis is a type of kidney inflammation that affects the tiny blood vessels in the glomeruli of the kidneys. This condition leads to damage to the kidneys' filtering system and can cause proteinuria, hematuria, and decreased kidney function.

Hereditary Nephropathy with Diffuse Mesangiocapillary Glomerulonephritis is inherited in an autosomal dominant pattern, which means that a person only needs to inherit one copy of the mutated gene from either parent to develop the condition.

  1. Signs and Symptoms
  2. The symptoms of Hereditary Nephropathy with Diffuse Mesangiocapillary Glomerulonephritis can vary from person to person. Some individuals may not even experience any symptoms until later in life. However, some common signs and symptoms include:

    • Proteinuria (excessive protein in the urine)
    • Hematuria (blood in the urine)
    • High blood pressure
    • Swelling in the legs and feet
    • Decreased kidney function
  3. Diagnosis
  4. Diagnosis of Hereditary Nephropathy with Diffuse Mesangiocapillary Glomerulonephritis involves a thorough medical history, physical examination, and laboratory tests. A urine test may be done to check for proteinuria and hematuria, while blood tests may be done to check for kidney function. Additional tests, such as a kidney biopsy or genetic testing, may also be performed to confirm the diagnosis.

  5. Treatment
  6. There is currently no cure for Hereditary Nephropathy with Diffuse Mesangiocapillary Glomerulonephritis. Treatment aims to manage symptoms and slow the progression of kidney damage. This may include medications to control blood pressure and reduce proteinuria, as well as dietary changes to reduce the workload on the kidneys.

  7. Conclusion
  8. Hereditary Nephropathy with Diffuse Mesangiocapillary Glomerulonephritis is a rare genetic disorder that affects the kidneys. While there is no cure, early diagnosis and treatment can help manage symptoms and slow the

    Treatment of Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis:

    Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis is a rare genetic disorder that affects the kidneys. This condition is characterized by the presence of abnormal proteins in the kidneys, which can cause damage and lead to kidney failure over time. While there is no cure for this condition, there are several treatment options available to help ma...

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