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威廉姆斯-贝伦综合征患儿的先天性泌尿生殖系统异常

Congenital genitourinary abnormalities in children with Williams-Beuren syndrome.

作者信息

Sammour Zein M, Gomes Cristiano M, de Bessa Jose, Pinheiro Marcello S, Kim Chong A E, Hisano Marcelo, Bruschini Homero, Srougi Miguel

机构信息

Division of Urology, University of Sao Paulo School of Medicine, Sao Paulo, Brazil.

Division of Urology, University of Sao Paulo School of Medicine, Sao Paulo, Brazil.

出版信息

J Pediatr Urol. 2014 Oct;10(5):804-9. doi: 10.1016/j.jpurol.2014.01.013. Epub 2014 Feb 13.

Abstract

OBJECTIVE

Williams-Beuren syndrome (WBS) is an autosomal dominant disorder caused by a gene deletion on chromosome 7q11.23. Patients with WBS usually show a group of features such as developmental delay, cardiovascular anomalies, mental retardation, and characteristic facial appearance. Abdominal wall defects, external genitalia anomalies, and structural abnormalities of the urinary tract have been scarcely evaluated and were the focus of our study.

MATERIALS AND METHODS

We prospectively evaluated 41 boys and 38 girls with WBS, with a mean age of 8.8 ± 4.1 (range 3-19 years). All patients were examined for the evaluation of inguinal and umbilical hernias and genital anomalies. All patients were offered a radiological evaluation, including urinary tract ultrasound, voiding cystourethrogram, and dimercaptosuccinic acid renal scintigraphy (DMSA scan).

RESULTS

Of the 41 boys, 30 (73.1%) had abnormalities on physical examination, including bilateral undescended testis in 13 (31.7%), retractile testis in four (9.7%), hypospadias in four (9.7%), and unilateral cryptorchidism in three (7.3%) patients. Of the 38 female subjects, 17 (44.7%) had at least one abnormality, including umbilical hernia in 11 (28.9%), unilateral inguinal hernia in four (10.5%), and bilateral inguinal hernia in three (7.8%) patients. Uroradiological abnormalities were found in 41 patients (51.9%). On sonography, six (7.6%) patients had unilateral hydronephrosis, three (3.8%) had a duplicated collecting system, and two (2.5%) had kidney stones. On DMSA, performed in 36 patients, four (11.1%) had unilateral renal scarring and two (5.5%) had bilateral renal scarring. Cystourethrography was obtained from 56 patients, of whom 27 (48.2%) had bladder diverticulum, 18 (32.1%) had bladder wall trabeculation, and three (5.3%) had vesicoureteral reflux. We found no association of urological abnormalities with cardiovascular defects.

CONCLUSIONS

Patients with WBS have a high prevalence of abdominal wall, external genitalia, and urological abnormalities, emphasizing the importance of proper physical examination and radiological investigation in this population.

摘要

目的

威廉姆斯-贝伦综合征(WBS)是一种常染色体显性疾病,由7号染色体q11.23区域的基因缺失引起。WBS患者通常表现出一系列特征,如发育迟缓、心血管异常、智力低下和特征性面容。腹壁缺陷、外生殖器异常和泌尿系统结构异常很少得到评估,而这正是我们研究的重点。

材料与方法

我们前瞻性评估了41名男孩和38名女孩,平均年龄为8.8±4.1岁(范围3 - 19岁)。所有患者均接受检查以评估腹股沟疝和脐疝以及生殖器异常情况。所有患者均接受了影像学评估,包括泌尿系统超声、排尿性膀胱尿道造影和二巯基丁二酸肾闪烁显像(DMSA扫描)。

结果

在41名男孩中,30名(73.1%)体格检查有异常,包括双侧隐睾13名(31.7%)、回缩性睾丸4名(9.7%)、尿道下裂4名(9.7%)以及单侧隐睾3名(7.3%)。在38名女性受试者中,17名(44.7%)至少有一项异常,包括脐疝11名(28.9%)、单侧腹股沟疝4名(10.5%)以及双侧腹股沟疝3名(7.8%)。41名患者(51.9%)发现有泌尿系统影像学异常。超声检查时,6名(7.6%)患者有单侧肾积水,3名(3.8%)有重复集合系统,2名(2.5%)有肾结石。在36名患者中进行的DMSA检查显示,4名(11.1%)有单侧肾瘢痕,2名(5.5%)有双侧肾瘢痕。56名患者进行了膀胱尿道造影,其中27名(48.2%)有膀胱憩室,18名(32.1%)有膀胱壁小梁形成,3名(5.3%)有膀胱输尿管反流。我们发现泌尿系统异常与心血管缺陷之间无关联。

结论

WBS患者腹壁、外生殖器和泌尿系统异常的发生率较高,这凸显了对该人群进行适当体格检查和影像学检查的重要性。

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