Oligohydramnion, renal failure and no pulmonary hypoplasia in glomerulocystic kidney disease

被引：5

作者：

Landau, D ^{[1
]}

Shalev, H ^{[1
]}

Shulman, H ^{[1
]}

Barki, Y ^{[1
]}

Maor, E ^{[1
]}

Zmora, E ^{[1
]}

机构：

[1] Soroka Med Ctr, Dept Pediat, IL-84101 Beer Sheva, Israel

来源：

PEDIATRIC NEPHROLOGY | 2000年 / 14卷 / 04期

关键词：

glomerulocystic kidney disease; oligohydramnion; renal failure-neonate; genetics;

D O I：

10.1007/s004670050767

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Two newborns with glomerulocystic kidney disease manifesting as late onset oligohydramnion and neonatal anuria, yet without severe respiratory distress, are presented. They had a similar perinatal course and associated clinical manifestations. No associated congenital or inherited malformation syndrome could be defined. Both infants' parents were first degree cousins and belonged to the same small Bedouin tribe, and neither they nor the infants' siblings had polycystic kidneys or renal insufficiency, pointing to either a possible genetic etiology or a common external toxic exposure.

引用

页码：319 / 321

页数：3

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