Evidence map›Paper›PMID 37957608›Full record

ArticleBMC medical genomics2023

Occurrence of mosaic trisomy 22 and pericentric inversion of chromosome 9 in a patient with a good prognosis.

Aline Nardelli, Larissa Valéria Laskoski, Andressa Fernanda Luiz, Maruhen Amir Datsch Silveira, Luciana Paula Grégio d'Arce

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 17% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. 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

5 authors at 2 institutions in 2 countries.

Aline NardelliHospital Universitário do Oeste do Paraná, Western Parana State University, Avenida Tancredo Neves 3224, Santo Onofre, Cascavel, Paraná, Brazil. alinenardellibio@gmail.com.
Larissa Valéria LaskoskiHospital Universitário do Oeste do Paraná, Western Parana State University, Avenida Tancredo Neves 3224, Santo Onofre, Cascavel, Paraná, Brazil.
Andressa Fernanda LuizHospital Universitário do Oeste do Paraná, Western Parana State University, Avenida Tancredo Neves 3224, Santo Onofre, Cascavel, Paraná, Brazil.
Maruhen Amir Datsch SilveiraCentre de Recherche sur le Cancer de l'Université Laval, 9 Rue McMahon, Québec, QC, G1R 3S3, Canadá.
Luciana Paula Grégio d'ArceHospital Universitário do Oeste do Paraná, Western Parana State University, Avenida Tancredo Neves 3224, Santo Onofre, Cascavel, Paraná, Brazil.
Universidade Estadual do Oeste do Paraná · BRUniversité Laval · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complete trisomy 22 is a rare chromosomal condition that is incompatible with life. However, mosaic trisomy 22 usually has prolonged survival compatibility and may present a good prognosis depending on the tissues affected. Herein, we described a male patient with the occurrence of mosaic trisomy 22 associated with the inversion of chromosome 9, with karyotype 47, XY, inv (9) (p11q13), + 22 [5] / 46, XY, inv(9) (p11q13) [45] and arr 22q11.1 ~ q13.33(16,417008-51,219,009)x2 ~ 3. It is not possible to infer, in general, the clinical characteristics associated with mosaic trisomy 22. However, the patient presented common clinical features observed in reported cases (in parentheses the percentage observed comparing all reported cases): facial dysmorphia (100%), delay in motor development/growth (82%), cardiac abnormalities (73%), ear abnormalities (55%) and facial and/or body asymmetry (55%), in addition to hypotonia, skin spots, hypoplastic nails. Given the survival and quality of life associated with multidisciplinary treatment, it can be concluded that the patient has a good prognosis. Conclusively, we're presenting the occurrence of mosaic trisomy 22 and chromosome 9 inversion in the patient with favorable prognosis. Thus, this study proposed a guide which should be inserted in databases of rare genetic conditions to help genetic counselors define mosaic trisomy 22 diagnosis.

Indexed as

MosaicismQuality of LifeChromosome InversionChromosomes, Human, Pair 22Chromosomes, Human, Pair 9HumansMaleTrisomyChromosome 22 trisomyChromosome abnormalitiesGenetic diagnosisMosaicism

Identifiers

PMID37957608
PMCPMC10644605
OpenAlexW4388627109

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.