Profile of patients with genitourinary anomalies treated in a clinical genetics service in the Brazilian unified health system

Ilanna Fragoso Peixoto Gazzaneo , Camila Maia Costa de Queiroz , Larissa Clara Vieira Goes , Victor José Correia Lessa , Reinaldo Luna de Omena Filho , Diogo Lucas Lima do Nascimento , Reginaldo José Petroli , Susane Vasconcelos Zanotti , Isabella Lopes Monlleó
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Abstract

Objective

To describe the profile of patients with genitourinary abnormalities treated at a tertiary hospital genetics service.

Methods

Cross-sectional study of 1068 medical records of patients treated between April/2008 and August/2014. A total of 115 cases suggestive of genitourinary anomalies were selected, regardless of age. A standardized clinical protocol was used, as well as karyotype, hormone levels and genitourinary ultrasound for basic evaluation. Laparoscopy, gonadal biopsy and molecular studies were performed in specific cases. Patients with genitourinary malformations were classified as genitourinary anomalies (GUA), whereas the others, as Disorders of Sex Differentiation (DSD). Chi-square, Fisher and Kruskal–Wallis tests were used for statistical analysis and comparison between groups.

Results

80 subjects met the inclusion criteria, 91% with DSD and 9% with isolated/syndromic GUA. The age was younger in the GUA group (p<0.02), but these groups did not differ regarding external and internal genitalia, as well as karyotype. Karyotype 46,XY was verified in 55% and chromosomal aberrations in 17.5% of cases. Ambiguous genitalia occurred in 45%, predominantly in 46,XX patients (p<0.006). Disorders of Gonadal Differentiation accounted for 25% and congenital adrenal hyperplasia, for 17.5% of the sample. Consanguinity occurred in 16%, recurrence in 12%, lack of birth certificate in 20% and interrupted follow-up in 31% of cases.

Conclusions

Patients with DSD predominated. Ambiguous genitalia and abnormal sexual differentiation were more frequent among infants and prepubertal individuals. Congenital adrenal hyperplasia was the most prevalent nosology. Younger patients were more common in the GUA group. Abandonment and lower frequency of birth certificate occurred in patients with ambiguous or malformed genitalia. These characteristics corroborate the literature and show the biopsychosocial impact of genitourinary anomalies.

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在巴西统一卫生系统的临床遗传学服务治疗的泌尿生殖系统异常患者的概况
目的了解某三级医院遗传科收治的泌尿生殖系统异常患者的情况。方法对2008年4月至2014年8月收治的1068例患者病历进行横断面分析。我们选择了115例提示泌尿生殖系统异常的病例,不论年龄大小。使用标准化的临床方案,以及核型,激素水平和泌尿生殖系统超声进行基本评估。腹腔镜检查,性腺活检和分子研究在特定情况下进行。泌尿生殖系统畸形归为泌尿生殖系统异常(GUA),其他归为性别分化障碍(DSD)。统计学分析和组间比较采用卡方检验、Fisher检验和Kruskal-Wallis检验。结果80例受试者符合纳入标准,91%为DSD, 9%为孤立性/综合征型GUA。GUA组年龄较小(p<0.02),但两组在外生殖器和内生殖器以及核型上没有差异。核型46、XY占55%,染色体畸变占17.5%。45%的患者出现生殖器模糊,主要发生在46,xx例患者(p<0.006)。性腺分化障碍占25%,先天性肾上腺增生占17.5%。有血缘关系的占16%,复发的占12%,缺乏出生证明的占20%,随访中断的占31%。结论以DSD患者为主。在婴儿和青春期前个体中,生殖器模糊和性别分化异常更为常见。先天性肾上腺增生是最常见的病因。年轻患者在GUA组中更为常见。生殖器官模糊或畸形的患者出现遗弃和较低的出生证明。这些特征证实了文献,并显示了泌尿生殖系统异常的生物心理社会影响。
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