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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade de Pediatria de São Paulo 2016
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.
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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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