Evidence map›Paper›PMID 26525685›Full record

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

[Prevalence of Y-chromosome sequences and gonadoblastoma in Turner syndrome].

Alessandra Bernadete Trovó de Marqui, Roseane Lopes da Silva-Grecco, Marly Aparecida Spadotto Balarin

Open access · diamondAbstract readReview
In one paragraph

Review 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. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Germ Cell Tumors in Dysgenetic Gonads.Clinics (Sao Paulo, Brazil) · 2019
    Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Approach to the Virilizing Girl at Puberty.The Journal of clinical endocrinology and metabolism · 2021
    Review
  7. Dysgerminoma with a Somatic Exon 17Diagnostics (Basel, Switzerland) · 2020
    Article
  8. Article
  9. Article
  10. Article
  11. The Use of FluorescenceJournal of human reproductive sciences
    Article
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

3 authors at 1 institution in 1 country.

Alessandra Bernadete Trovó de MarquiUniversidade Federal do Triângulo Mineiro (UFTM), Uberaba, MG, Brasil. Electronic address: alessandratrovo@hotmail.com.
Roseane Lopes da Silva-GreccoUniversidade Federal do Triângulo Mineiro (UFTM), Uberaba, MG, Brasil.
Marly Aparecida Spadotto BalarinUniversidade Federal do Triângulo Mineiro (UFTM), Uberaba, MG, Brasil.
Universidade Federal do Triângulo Mineiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess the prevalence of Y-chromosome sequences and gonadoblastoma in patients with Turner syndrome using molecular techniques. DATA SOURCE: A literature search was performed in Pubmed, limiting the period of time to the years 2005 to 2014 and using the descriptors: Turner syndrome and Y sequences (n=26), and Turner syndrome and Y-chromosome material (n=27). The inclusion criteria were: articles directly related to the subject and published in English or Portuguese. Articles which did not meet these criteria and review articles were excluded. After applying these criteria, 14 papers were left. DATA SYNTHESIS: the main results regarding the prevalence of Y-chromosome sequences in Turner syndrome were: 1-about 60% of the studies were conducted by Brazilian researchers; 2-the prevalence varied from 4.6 to 60%; 3-the most frequently investigated genes were SRY, DYZ3 and TSPY; 4-seven studies used only PCR, while in the remaining seven it was associated with FISH. Nine of the 14 studies reported gonadectomy and gonadoblastoma. The highest prevalence of gonadoblastoma (33%) was found in two studies. In five out of the nine papers evaluated the prevalence of gonadoblastoma was 10 to 25%; in two of them it was zero.

conclusionsaccording to these data, molecular analysis to detect Y-chromosome sequences in TS patients is indicated, regardless of their karyotype. In patients who test positive for these sequences, gonadoblastoma needs to be investigated.

Indexed as

Chromosomes, Human, YFemaleGonadoblastomaHumansKaryotypingOvarian NeoplasmsSequence Analysis, DNATurner SyndromeCromossomo YDisgenesia gonadalGonadal dysgenesisGonadoblastomaPolymerase chain reactionPrevalencePrevalênciaReação em cadeia da polimeraseSíndrome de TurnerTurner syndromeY chromosome

Identifiers

PMID26525685
PMCPMC4795730
OpenAlexW1953113384

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.