Evidence map›Paper›PMID 26985348›Full record

ArticleInternational journal of fertility & sterility

Molecular Dissection Using Array Comparative Genomic Hybridization and Clinical Evaluation of An Infertile Male Carrier of An Unbalanced Y;21 Translocation: A Case Report and Review of The Literature.

Alfredo Orrico, Giuseppina Marseglia, Chiara Pescucci, Ambra Cortesi, Paola Piomboni, Andrea Giansanti, Francesca Gerundino, Roberto Ponchietti

Open access · greenAbstract read
In one paragraph

Article in International journal of fertility & sterility. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. An Infertile Azoospermic Male With 45, X T(Yp;15) Karyotype.Journal of family & reproductive health · 2021
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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

8 authors at 2 institutions in 1 country.

Alfredo OrricoMolecular Medicine Unit, Azienda Ospedaliera Universitaria Senese, Siena, Italy; Medical Genetics, Misericordia Hospital, Grosseto, Italy.
Giuseppina MarsegliaDiagnostic Genetic Unit, Department of Laboratory, Careggi University Hospital, Firenze, Italy.
Chiara PescucciDiagnostic Genetic Unit, Department of Laboratory, Careggi University Hospital, Firenze, Italy.
Ambra CortesiMedical Genetics, Misericordia Hospital, Grosseto, Italy.
Paola PiomboniDepartment of Molecular and Developmental Medicine, University of Siena, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
Andrea GiansantiGenitourinary Unit, University of Siena, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
Francesca GerundinoDiagnostic Genetic Unit, Department of Laboratory, Careggi University Hospital, Firenze, Italy.
Roberto PonchiettiGenitourinary Unit, University of Siena, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
Azienda Ospedaliero-Universitaria Careggi · ITOspedale Misericordia - Grosseto · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromosomal defects are relatively frequent in infertile men however, translocations between the Y chromosome and autosomes are rare and less than 40 cases of Y-autosome translocation have been reported. In particular, only three individuals has been described with a Y;21 translocation, up to now. We report on an additional case of an infertile man in whom a Y;21 translocation was associated with the deletion of a large part of the Y chromosome long arm. Applying various techniques, including conventional cytogenetic procedures, fluorescence in situ hybridisation (FISH) analysis and array comparative genomic hybridization (array-CGH) studies, we identified a derivative chromosome originating from a fragment of the short arm of the chromosome Y translocated on the short arm of the 21 chromosome. The Y chromosome structural rearrangement resulted in the intactness of the entire short arm, including the sex-determining region Y (SRY) and the short stature homeobox (SHOX) loci, although translocated on the 21 chromosome, and the loss of a large part of the long arm of the Y chromosome, including azoospermia factor-a (AZFa), AZFb, AZFc and Yq heterochromatin regions. This is the first case in which a (Yp;21p) translocation has been ascertained using an array-CGH approach, thus reporting details of such a rearrangement at higher resolution.

Indexed as

AzoospermiaHypogonadismTranslocationY Chromosome

Identifiers

PMID26985348
PMCPMC4793181
OpenAlexW2296950348

What OpenQuestion holds

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LicenceCC BY
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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.