HEREDITARY NEPHRITIS - RE-EXAMINATION OF ITS CLINICAL AND GENETIC FEATURES

被引:62
作者
ONEILL, WM
ATKIN, CL
BLOOMER, HA
机构
[1] UNIV UTAH, COLL MED, DEPT INTERNAL MED, DIV KIDNEY DIS, SALT LAKE CITY, UT 84112 USA
[2] UNIV UTAH, COLL MED, DEPT INTERNAL MED, DIV HEMATOL ONCOL, SALT LAKE CITY, UT 84112 USA
关键词
D O I
10.7326/0003-4819-88-2-176
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In order to re-evaluate current concepts of hereditary nephritis the authors studied the urinary findings, the course of the disease, and its genetic transmission in two large pedigrees. We identified 150 patients with hereditary nephritis. Our data show that microscopic hematuria is the most reliable urinary criterion for diagnosing hereditary nephritis in both male and female patients. The hematuria is frequently accompanied by erythrocyte casts indicating that the renal lesion is a glomerulitis. Men are more severely affected than women. They have striking urinary abnormalities, which are present in early childhood, and they progress to renal failure in adult life. Affected women have less obvious urinary abnormalities and rarely develop uremia. In these two families a sex-linked dominant mode of genetic transmission was present. The demonstration that hereditary nephritis is X-linked, at least in some families, helps to explain the difference in severity between men and women and the variable expression among affected women.
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页码:176 / 182
页数:7
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