Evidence map›Paper›PMID 36064700›Full record

ReviewBMC medical genomics2022

Duplication of SOX3 in an SRY-negative 46,XX male with prostatic utricle: case report and literature review.

Jiansheng Wei, Changrong Liu, Minyan Zhang, Shen Liu, Junjie Fu, Peng Lin

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in BMC medical genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

12 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Cytogenomic Investigation of Individuals with Ovotesticular Difference of Sex Development.Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation · 2026
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
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

6 authors at 1 institution in 1 country.

Jiansheng WeiDepartment of Pediatric Urology, Fuzhou Children's Hospital of Fujian Province, 145 Ba-yi-qi road, Fuzhou, Fujian Province, China. wjs0831169@outlook.com.ORCID 0000-0001-7809-0577
Changrong LiuDepartment of Pediatric Urology, Fuzhou Children's Hospital of Fujian Province, 145 Ba-yi-qi road, Fuzhou, Fujian Province, China.
Minyan ZhangDepartment of Pediatric Urology, Fuzhou Children's Hospital of Fujian Province, 145 Ba-yi-qi road, Fuzhou, Fujian Province, China.
Shen LiuDepartment of Pediatric Urology, Fuzhou Children's Hospital of Fujian Province, 145 Ba-yi-qi road, Fuzhou, Fujian Province, China.
Junjie FuDepartment of Pediatric Urology, Fuzhou Children's Hospital of Fujian Province, 145 Ba-yi-qi road, Fuzhou, Fujian Province, China.
Peng LinDepartment of Pediatric Urology, Fuzhou Children's Hospital of Fujian Province, 145 Ba-yi-qi road, Fuzhou, Fujian Province, China.
Fujian Women and Children Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background46,XX male disorders of sex development are rare. Approximately 80% of cases of testicular tissue differentiation may be due to translocation of SRY to the X chromosome or an autosome. SRY-negative 46,XX males show overexpression of pro-testis genes, such as SOX9 and SOX3, or failure of pro-ovarian genes, such as WNT4 and RSPO1, which induces testis differentiation, however, almost all testicles exhibit dysgenesis. Following inadequate exposure to androgens during the embryo stage, remnants of the Mullerian duct and incomplete closure of the urogenital sinus lead to enlargement of prostatic utricles. This condition is associated with proximal hypospadias and disorders of sex development. Many cases are asymptomatic, but show increased rates of postoperative complications and surgical failure. CASE PRESENTATION: A 5-year-old Chinese boy with scrotal hypospadias and bilateral cryptorchidism with prostatic utricles was presented. Gonadal histology showed ovo-testicular tissue on the right side and testicular tissue on the left side; all testicular tissue exhibited dysgenesis. Furthermore, chromosome karyotype analysis revealed 46,XX and, the presence of SRY was ruled out by polymerase chain reaction analysis. Whole-genome analysis showed the boy has a 1.4-Mb duplication in the Xq27.1q27.2 region (arr[hg19]Xq27.1q27.2:139585794-140996652) involving SOX3. No SOX3 duplication was observed in the parents, who had a normal phenotype.

conclusionsWe report the first case of an SRY-negative 46 XX male with prostatic utricle caused by SOX3 duplication. SOX3 duplication may cause sex reversal, and all 46,XX SRY-negative males should be screened for SOX3 mutations. Gonadal biopsy is recommended to evaluate ovarian and testicular tissue development. Testicular dysgenesis and low exposure to male hormones during fetal development can lead to enlarged prostatic utricles. Thus endoscopic examination should be performed preoperatively to detect prostatic utricles in SRY-negative 46,XX males to determine the surgical plan and reduce postoperative complications.

Indexed as

Disorders of Sex DevelopmentHypospadiasHumansMalePostoperative ComplicationsSaccule and UtricleSOXB1 Transcription FactorsTestisSOX3 protein, humanSOXB1 Transcription FactorsCase reportDisorder of sex developmentProstatic utricleSOX3

Identifiers

PMID36064700
PMCPMC9446824
OpenAlexW4294690484

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.