Hereditary nephritis
Hereditary Nephritis | |
---|---|
Synonyms | N/A |
Pronounce | N/A |
Specialty | N/A |
Symptoms | Hematuria, Proteinuria, Hypertension |
Complications | Chronic kidney disease, End-stage renal disease |
Onset | Childhood or adolescence |
Duration | Lifelong |
Types | N/A |
Causes | Genetic mutation |
Risks | Family history |
Diagnosis | Genetic testing, Kidney biopsy |
Differential diagnosis | N/A |
Prevention | N/A |
Treatment | Supportive care, Dialysis, Kidney transplant |
Medication | N/A |
Prognosis | N/A |
Frequency | Rare |
Deaths | N/A |
Hereditary Nephritis is a group of genetic disorders that affect the kidneys. It is characterized by hematuria (blood in the urine), proteinuria (protein in the urine), and often leads to chronic kidney disease and end-stage renal disease.
Causes[edit | edit source]
Hereditary Nephritis is caused by genetic mutations that affect the glomerular basement membrane of the kidneys. The most common form is Alport syndrome, which is caused by mutations in the COL4A3, COL4A4, or COL4A5 genes.
Symptoms[edit | edit source]
The symptoms of Hereditary Nephritis can vary but often include:
- Hematuria
- Proteinuria
- Hypertension
- Hearing loss (in some forms like Alport syndrome)
- Eye abnormalities
Diagnosis[edit | edit source]
Diagnosis of Hereditary Nephritis typically involves:
- Genetic testing to identify mutations
- Kidney biopsy to examine the glomerular basement membrane
- Urinalysis to detect hematuria and proteinuria
Treatment[edit | edit source]
There is no cure for Hereditary Nephritis, but treatment focuses on managing symptoms and slowing progression. Options include:
- Supportive care
- Blood pressure control
- Dialysis for kidney failure
- Kidney transplant
Prognosis[edit | edit source]
The prognosis for individuals with Hereditary Nephritis varies depending on the specific genetic mutation and the severity of the disease. Early diagnosis and management can improve outcomes.
See also[edit | edit source]
References[edit | edit source]
External links[edit | edit source]
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Contributors: Prab R. Tumpati, MD