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Profile of patients with genitourinary anomalies treated in a clinical genetics service in the Brazilian unified health system
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 w...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade de Pediatria de São Paulo
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795727/ https://www.ncbi.nlm.nih.gov/pubmed/26522823 http://dx.doi.org/10.1016/j.rppede.2015.06.024 |
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author | Gazzaneo, Ilanna Fragoso Peixoto de Queiroz, Camila Maia Costa Goes, Larissa Clara Vieira Lessa, Victor José Correia de Omena, Reinaldo Luna do Nascimento, Diogo Lucas Lima Petroli, Reginaldo José Zanotti, Susane Vasconcelos Monlleó, Isabella Lopes |
author_facet | Gazzaneo, Ilanna Fragoso Peixoto de Queiroz, Camila Maia Costa Goes, Larissa Clara Vieira Lessa, Victor José Correia de Omena, Reinaldo Luna do Nascimento, Diogo Lucas Lima Petroli, Reginaldo José Zanotti, Susane Vasconcelos Monlleó, Isabella Lopes |
author_sort | Gazzaneo, Ilanna Fragoso Peixoto |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4795727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Sociedade de Pediatria de São Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-47957272016-04-01 Profile of patients with genitourinary anomalies treated in a clinical genetics service in the Brazilian unified health system Gazzaneo, Ilanna Fragoso Peixoto de Queiroz, Camila Maia Costa Goes, Larissa Clara Vieira Lessa, Victor José Correia de Omena, Reinaldo Luna do Nascimento, Diogo Lucas Lima Petroli, Reginaldo José Zanotti, Susane Vasconcelos Monlleó, Isabella Lopes Rev Paul Pediatr Original Articles 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. Sociedade de Pediatria de São Paulo 2016 /pmc/articles/PMC4795727/ /pubmed/26522823 http://dx.doi.org/10.1016/j.rppede.2015.06.024 Text en © 2015 Sociedade de Pediatria de São Paulo. Published by Elsevier Editora Ltda http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Gazzaneo, Ilanna Fragoso Peixoto de Queiroz, Camila Maia Costa Goes, Larissa Clara Vieira Lessa, Victor José Correia de Omena, Reinaldo Luna do Nascimento, Diogo Lucas Lima Petroli, Reginaldo José Zanotti, Susane Vasconcelos Monlleó, Isabella Lopes Profile of patients with genitourinary anomalies treated in a clinical genetics service in the Brazilian unified health system |
title | Profile of patients with genitourinary anomalies treated in a clinical
genetics service in the Brazilian unified health system |
title_full | Profile of patients with genitourinary anomalies treated in a clinical
genetics service in the Brazilian unified health system |
title_fullStr | Profile of patients with genitourinary anomalies treated in a clinical
genetics service in the Brazilian unified health system |
title_full_unstemmed | Profile of patients with genitourinary anomalies treated in a clinical
genetics service in the Brazilian unified health system |
title_short | Profile of patients with genitourinary anomalies treated in a clinical
genetics service in the Brazilian unified health system |
title_sort | profile of patients with genitourinary anomalies treated in a clinical
genetics service in the brazilian unified health system |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795727/ https://www.ncbi.nlm.nih.gov/pubmed/26522823 http://dx.doi.org/10.1016/j.rppede.2015.06.024 |
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