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胎儿常染色体显性多囊肾病

Autosomal dominant polycystic kidney disease in the fetus.

作者信息

Michaud J, Russo P, Grignon A, Dallaire L, Bichet D, Rosenblatt D, Lamothe E, Lambert M

机构信息

Department of Pediatrics, Hôpital Sainte-Justine, Montréal, Québec, Canada.

出版信息

Am J Med Genet. 1994 Jul 1;51(3):240-6. doi: 10.1002/ajmg.1320510314.

Abstract

We report on 3 cases with a fetal presentation of autosomal dominant polycystic kidney disease (ADPKD), which illustrate the variable expression of ADPKD during fetal life. Fetus 1 was diagnosed at 20 weeks of gestation by ultrasonography; a molecular prenatal diagnosis was performed at 10 weeks on fetus 2, a sib of fetus 1; and ADPKD was an incidental finding in fetus 3 who was aborted at 16 weeks for anencephaly. All pregnancies were terminated and pathologic studies of the fetal kidneys were performed. From these cases and a review of the literature, we draw the following conclusions: (1) so far, all fetal ADPKD kidneys that have been histologically studied have shown cystic dilatations; 28/32 of these fetuses had ultrasonographic manifestations of the disease and/or had sibs with an early-onset form of it; (2) these cysts can be found in newly formed nephrons (fetus 2), predominantly in the more mature nephrons of the deep cortex (fetus 1) or more sparsely distributed in the cortex (fetus 3); these different patterns may reflect different rates of progression of the disease; (3) in contrast to the histologic findings in adult kidneys, glomeruli seem to be predominantly affected in fetal ADPKD; (4) severe fetal expression of ADPKD seems to cluster in some families; and (5) so far, all DNA analyses performed in families with subjects presenting during the fetal or neonatal period have been consistent with linkage to the PKD1 locus.

摘要

我们报告了3例胎儿期表现为常染色体显性多囊肾病(ADPKD)的病例,这些病例说明了ADPKD在胎儿期的不同表现形式。胎儿1在妊娠20周时通过超声检查确诊;对胎儿2(胎儿1的同胞)在妊娠10周时进行了分子产前诊断;胎儿3因无脑儿在16周时流产,ADPKD是偶然发现。所有妊娠均终止,并对胎儿肾脏进行了病理研究。从这些病例以及文献回顾中,我们得出以下结论:(1)迄今为止,所有经组织学研究的胎儿ADPKD肾脏均显示有囊性扩张;这些胎儿中有28/32有该疾病的超声表现和/或有早发型的同胞;(2)这些囊肿可在新形成的肾单位中发现(胎儿2),主要在深层皮质较成熟的肾单位中(胎儿1),或在皮质中分布较稀疏(胎儿3);这些不同模式可能反映了疾病的不同进展速度;(3)与成人肾脏的组织学发现不同,胎儿ADPKD中肾小球似乎是主要受累部位;(4)ADPKD的严重胎儿期表现似乎在一些家族中聚集;(5)迄今为止,在有胎儿期或新生儿期发病个体的家族中进行的所有DNA分析均与PKD1位点连锁一致。

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