Evidence map›Paper›PMID 26522823›Full record

ArticleRevista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo

[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

Open access · hybridAbstract read
In one paragraph

Article in Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 91% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Ilanna Fragoso Peixoto GazzaneoUniversidade Federal de Alagoas (Ufal), Maceió, AL, Brasil.
Camila Maia Costa de QueirozUniversidade Federal de Alagoas (Ufal), Maceió, AL, Brasil.
Larissa Clara Vieira GoesUniversidade Federal de Alagoas (Ufal), Maceió, AL, Brasil.
Victor José Correia LessaUniversidade Federal de Alagoas (Ufal), Maceió, AL, Brasil.
Reinaldo Luna de Omena FilhoUniversidade Estadual de Ciências da Saúde de Alagoas (Uncisal), Maceió, AL, Brasil.
Diogo Lucas Lima do NascimentoUniversidade Estadual de Ciências da Saúde de Alagoas (Uncisal), Maceió, AL, Brasil.
Reginaldo José PetroliUniversidade Federal de Alagoas (Ufal), Maceió, AL, Brasil.
Susane Vasconcelos ZanottiUniversidade Federal de Alagoas (Ufal), Maceió, AL, Brasil.
Isabella Lopes MonlleóUniversidade Federal de Alagoas (Ufal), Maceió, AL, Brasil. Electronic address: isabella.monlleo@gmail.com.
Universidade Federal de Alagoas · BRUniversidade Estadual de Ciências da Saúde de Alagoas · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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

methodsCross-sectional study of 1,068 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 sex differentiation disorders (SDD). Chi-square, Fisher and Kruskal-Wallis tests were used for statistical analysis and comparison between groups.

results80 subjects met the inclusion criteria, 91% with SDD 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). Gonadal differentiation disorders 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.

conclusionsPatients with SDD 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.

Indexed as

AdolescentAdrenal Hyperplasia, CongenitalAdultBrazilChildChild, PreschoolCross-Sectional StudiesDisorders of Sex DevelopmentFemaleHormonesHumansInfantInfant, NewbornKaryotypeMaleUrogenital AbnormalitiesHormonesDiferenciação sexual/genéticaEtiologiaEtiologyGenitaliaGenitáliaSexual differentiation/genetics

Identifiers

PMID26522823
PMCPMC4795727
OpenAlexW2279108403

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.