2 BROTHERS WITH IDIOPATHIC MEMBRANOUS NEPHROPATHY AND FAMILIAL SENSORINEURAL DEAFNESS

被引：12

作者：

MERONI, M

VOLPI, A

USBERTI, M

BATTINI, G

TARELLI, LT

GIORDANO, F

SESSA, A

机构：

[1] OSPED VIMERCATE,UNITA OPERAT NEFROL & DIALISI,VIA C BATTISTI 23,I-20059 VIMERCATE,ITALY

[2] OSPED VIMERCATE,SERV ANAT PATOL,I-20059 VIMERCATE,ITALY

[3] OSPED LENO,SERV NEFROL & DIALISI,LENO,ITALY

[4] UNIV MILAN,IST ANAT UMANA NORMALE,I-20122 MILAN,ITALY

来源：

AMERICAN JOURNAL OF KIDNEY DISEASES | 1990年 / 15卷 / 03期

关键词：

familial nephropathy; HLA antigens; Idiopathic membranous nephropathy; nerve deafness;

D O I：

10.1016/S0272-6386(12)80773-6

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 [临床医学]; 100201 [内科学];

摘要：

Genetic factors could play an important role in the pathogenesis of idiopathic membranous nephropathy, and a few cases of familial membranous nephropathy have been described: an increased incidence of some HLA antigens as DR3 and others has been reported. We present two brothers with idiopathic membranous nephropathy and sensorineural deafness. HLA typing was performed in the two patients and in the members of the family, and it showed the absence of linkage of an HLA antigen with the renal disease in the family. © 1990, National Kidney Foundation, Inc.. All rights reserved.

引用

页码：269 / 272

页数：4

共 16 条

[1]

BERTOUX FC, 1984, CLIN NEPHROL, V21, P15

[2]

CAMERON JS, 1979, KIDNEY INT, V15, P88

[3]

GENETIC-HETEROGENEITY OF ALPORT SYNDROME [J].