Rosipal S, Fukal J, Dolezel L
Detské oddelenie NsP Poprad.
Cesk Pediatr. 1991 Mar;46(3):153-5.
The authors submit the description of two sisters with hereditary nephropathy, with symptoms of nephrotic syndrome. In the clinical picture dominated permanent anuria, rapid renal failure and death at the end of neonatal age. Histopathological findings classified the disease as infantile diffuse mesangial sclerosis. The third patient is a sporadic case of primary congenital nephrotic syndrome.
作者报告了两例患有遗传性肾病且伴有肾病综合征症状的姐妹病例。临床表现以持续性无尿、快速肾衰竭以及在新生儿期末死亡为主。组织病理学检查结果将该疾病归类为婴儿弥漫性系膜硬化。第三例患者是原发性先天性肾病综合征的散发病例。
