Evidence map›Paper›PMID 35405793›Full record

ArticleAnimals : an open access journal from MDPI2022

The Second Case of Non-Mosaic Trisomy of Chromosome 26 with Homologous Fusion 26q;26q in the Horse.

Sharmila Ghosh, Josefina Kjöllerström, Laurie Metcalfe, Stephen Reed, Rytis Juras, Terje Raudsepp

Open access · goldAbstract readCase Reports
In one paragraph

Article in Animals : an open access journal from MDPI, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 25% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

6 authors at 2 institutions in 1 country.

Sharmila GhoshDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0001-9539-8290
Josefina KjöllerströmDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0001-9390-4153
Laurie MetcalfeRood & Riddle Equine Hospital, Lexington, KY 40580, USA.
Stephen ReedRood & Riddle Equine Hospital, Lexington, KY 40580, USA.
Rytis JurasDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0002-7385-0618
Terje RaudseppDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0003-2276-475X
Texas A&M University · USRood and Riddle Equine Hospital · US

Funding

Texas A&M Molecular Cytogenetics and Animal Genetics Laboratories na
6 · The paper itself

Abstract

We present cytogenetic and genotyping analysis of a Thoroughbred foal with congenital neurologic disorders and its phenotypically normal dam. We show that the foal has non-mosaic trisomy for chromosome 26 (ECA26) but normal 2n = 64 diploid number because two copies of ECA26 form a metacentric derivative chromosome der(26q;26q). The dam has normal 64,XX karyotype indicating that der(26q;26q) in the foal originates from errors in parental meiosis or post-fertilization events. Genotyping ECA26 microsatellites in the foal and its dam suggests that trisomy ECA26 is likely of maternal origin and that der(26q;26q) resulted from Robertsonian fusion. We demonstrate that conventional and molecular cytogenetic approaches can accurately identify aneuploidy with a derivative chromosome but determining the mechanism and parental origin of the rearrangement requires genotyping with chromosome-specific polymorphic markers. Most curiously, this is the second case of trisomy ECA26 with der(26q;26q) in the horse, whereas all other equine autosomal trisomies are 'traditional' with three separate chromosomes. We discuss possible ECA26 instability as a contributing factor for the aberration and likely ECA26-specific genetic effects on the clinical phenotype. Finally, because ECA26 shares evolutionary homology with human chromosome 21, which trisomy causes Down syndrome, cytogenetic, molecular, and phenotypic similarities between trisomies ECA26 and HSA21 are discussed.

Indexed as

congenital abnormalitiesDown syndromeFISHkaryotypingneurologic disordersparental originSTR genotyping

Identifiers

PMID35405793
PMCPMC8996834
OpenAlexW4220814915

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.