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在罕见的童年综合征中,泌尿系统问题的回顾性评估
Sevim Yener1, Ceyhan Şahin2, Zekeriya Ilce2
1Department of Pediatric Urology, University of Health Sciences, Umraniye Training and Research Hospital, Istanbul, TUR.
患有罕见综合征的儿科患者往往具有相关的泌尿器 anomalies. 建议对所有罕见综合征患者进行早期泌尿学评估,即使是没有症状的患者,以检测潜在的问题.
科学领域:
- 儿科泌尿外科 儿科泌尿外科
- 罕见疾病 罕见疾病
- 医学遗传学 医学遗传学
背景情况:
- 罕见综合征影响着少数人群,在全球范围内有不同的定义.
- 泌尿器官异常可能与罕见综合征有关,需要进行调查.
研究的目的:
- 为了调查患有罕见综合征的儿科患者尿道异常的患病率.
- 确定所有罕见综合征患者需要泌尿学评估的必要性.
主要方法:
- 对32名患有罕见综合征的儿科患者的回顾性分析,这些患者被转诊到儿科泌尿外科诊所 (2017-2022年).
- 审查尿道系统和囊超声波的发现.
- 详细的病史,包括并发症,疾病和手术.
主要成果:
- 在32名患者中,有10人 (31.2%) 呈现出病理性尿道系统超声检查结果.
- 确定的综合征包括微删除综合征 (n=4),罗伯茨综合征 (n=3),埃勒斯-丹洛斯综合征 (n=2).
- 发现了尿道异常,如水性和外皮,有时在无症状患者中发现.
结论:
- 尿道异常存在于儿童罕见综合征患者的很大一部分.
- 建议对所有罕见综合征患者进行例行泌尿检查,无论症状如何.
- 早期发现和管理泌尿病问题可以改善患者的治疗结果.
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