Incidence and spectrum of renal abnormalities in Williams-Beuren syndrome

被引:0
|
作者
Pankau, R
Partsch, CJ
Winter, M
Gosch, A
Wessel, A
机构
[1] CHRISTIAN ALBRECHTS UNIV KIEL, DEPT PEDIAT, W-2300 KIEL, GERMANY
[2] CHRISTIAN ALBRECHTS UNIV KIEL, DEPT OPHTHALMOL, W-2300 KIEL, GERMANY
[3] UNIV GOTTINGEN, DEPT PEDIAT CARDIOL, GOTTINGEN, GERMANY
[4] UNIV MUNSTER, INST REPROD MED, W-4400 MUNSTER, GERMANY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1996年 / 63卷 / 01期
关键词
Williams-Beuren syndrome; renal abnormalities; ultrasonography;
D O I
10.1002/(SICI)1096-8628(19960503)63:1<301::AID-AJMG49>3.0.CO;2-P
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Kidneys and urinary tract were examined systematically by ultrasonography in 130 patients with Williams-Beuren syndrome (59 females, median age 5.5 years; 71 males, median age 6.4 years). In addition, serum creatinine was determined and an analysis was performed, Creatinine clearance was available in 79 patients. Renal angiographic examinations were done in 18 patients, 8 of whom had renal artery narrowing (44%). The incidence of renal anomalies in Williams-Beuren syndrome was 17.7% vs, around 1.5% in the normal population (P < 0.0003). The spectrum of these anomalies ranged from minor anomalies such as bladder diverticula to more severe malformations such as renal aplasia or hypoplasia (in 5 of 130 patients), In nine patients a duplicated kidney was found, A decreased creatinine clearance (two patients), recurrent symptomatic urinary tract infections (four patients), and hypertension were uncommon, Nephrocalcinosis was not found in our patients. Our data demonstrate that the risk of a structural abnormality of the kidneys and the urinary tract is increased 12- to 36-fold in Williams-Beuren syndrome compared to the normal population, Ultrasound screening of the renal system should be part of the first evaluation of WBS patients. (C) 1996 Wiley-Liss, Inc.
引用
收藏
页码:301 / 304
页数:4
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