MUSCULAR HYPERTROPHY OF THE ESOPHAGUS AND ALPORT-LIKE GLOMERULAR-LESIONS IN A BOY

被引：24

作者：

LEGIUS, E

PROESMANS, W

VANDAMME, B

GEBOES, K

LERUT, T

EGGERMONT, E

机构：

[1] CATHOLIC UNIV LEUVEN,HOSP GASTHUISBERG,DEPT PAEDIAT,HEREST 49,B-3000 LOUVAIN,BELGIUM

[2] CATHOLIC UNIV LEUVEN,HOSP GASTHUISBERG,DEPT PATHOL,B-3000 LOUVAIN,BELGIUM

[3] CATHOLIC UNIV LEUVEN,HOSP GASTHUISBERG,DEPT SURG,B-3000 LOUVAIN,BELGIUM

来源：

EUROPEAN JOURNAL OF PEDIATRICS | 1990年 / 149卷 / 09期

关键词：

Alport syndrome; Autosomal dominant inheritance; Glomerulonephritis; Leiomyomatosis; Oesophageal muscular hypertrophy;

D O I：

10.1007/BF02034748

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

A patient with idiopathic muscular hypertrophy of the oesophagus, bilateral cataracts and an Alport-like nephropathy is described. Only 15 patients with a similar association have been described so far and autosomal dominant inheritance is most likely. © 1990 Springer-Verlag.

引用

页码：623 / 627

页数：5