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Benign hereditary nephritis

A S Peterson, J J Schubert

    The Journal of Family Practice
    |March 1, 1977
    PubMed
    Summary
    This summary is machine-generated.

    Hereditary nephritis, a kidney disease, may not always progress and can be detected in families with hematuria. Early family testing can reveal cases, even without a clear history of kidney issues.

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    Area of Science:

    • Nephrology
    • Genetics
    • Internal Medicine

    Background:

    • Glomerulonephritis diagnosis, prognosis, and heredity were studied in a large family.
    • Understanding hereditary nephritis is crucial for early detection and management.
    • Family history and clinical presentation are key indicators.

    Purpose of the Study:

    • To determine the diagnosis, prognosis, and heredity of glomerulonephritis within a single family across five generations.
    • To identify potential diagnostic markers and patterns of inheritance.
    • To assess the progression and mortality associated with hereditary nephritis.

    Main Methods:

    • A comprehensive study of 207 family members over five generations.
    • Clinical evaluation, including assessment of renal function and associated conditions.

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  • Family history collection focusing on urinary tract infections, hematuria, and hearing loss.

    • Main Results:

    • No significant renal insufficiency or renal-associated mortality was observed in the studied family.
    • 58% of individuals with hematuria reported a history of urinary tract infections.
    • Associated conditions included high-frequency hearing loss and elevated serum creatinine in some individuals.

    Conclusions:

    • Hereditary nephritis is not invariably a progressive renal disease.
    • Testing families of patients with benign recurrent hematuria, even without obvious kidney disease history, can lead to discovery.
    • Early identification through family screening is recommended for potential cases.