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Original Contribution  |   July 1992
Familial glomerular disease with asymptomatic Proteinuria and nephrotic syndrome: a new clinical entity
Article Information
Original Contribution   |   July 1992
Familial glomerular disease with asymptomatic Proteinuria and nephrotic syndrome: a new clinical entity
The Journal of the American Osteopathic Association, July 1992, Vol. 92, 875. doi:https://doi.org/10.7556/jaoa.1992.92.7.875
The Journal of the American Osteopathic Association, July 1992, Vol. 92, 875. doi:https://doi.org/10.7556/jaoa.1992.92.7.875
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Abstract

Seventy-three members of a 100-member kindred with asymptomatic proteinuria, nephrotic syndrome, and progressive renal failure were studied. Of those studied, 11 members had progressed to end-stage renal disease and seven had significant proteinuria (> 1 g/24 hours) with normal renal function. The genetic mode of inheritance was autosomal dominant with variable penetrance and expressivity. Histopathologic changes were variable but included focal segmental glomerulosclerosis and diffuse glomerulosclerosis. Renal failure usually occurred in the fifth decade of life. The most consistent clinical finding was proteinuria without microscopic hematuria or other significant urinary sediment elements. This disease differed from Alport's hereditary nephritis and congenital nephrotic syndrome in age of onset, urinary findings, and associated conditions, that is, nerve deafness. The hereditary proteinuria and nephrotic syndrome described in this kindred represents another facet in the spectrum of hereditary renal disease.