Evidence map›Paper›PMID 34602959›Full record

ArticleMolecular syndromology2021

An Apparently Balanced Complex Chromosome Rearrangement Involving Seven Breaks and Four Chromosomes in a Healthy Female and Segregation/Recombination in Her Affected Son.

Ana Eduarda Campos, Carla Rosenberg, Ana Krepischi, Marina França, Vanessa Lopes, Viviane Nakano, Tânia Vertemati, Marcos Cochak, Michele Migliavacca, Fernanda Milanezi and 7 more

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Molecular syndromology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

17 authors at 2 institutions in 1 country.

Ana Eduarda CamposDepartment of Clinical Genetics, Federal University of São Paulo, São Paulo, Brazil.
Carla RosenbergGeneOne, São Paulo, Brazil.
Ana KrepischiDepartment of Genetics and Evolutionary Biology, Institute of Biosciences, Human Genome and Stem Cell Research Center, University of São Paulo, São Paulo, Brazil.
Marina FrançaDepartment of Clinical Genetics, Federal University of São Paulo, São Paulo, Brazil.
Vanessa LopesGeneOne, São Paulo, Brazil.
Viviane NakanoGeneOne, São Paulo, Brazil.
Tânia VertematiPrivate Genetics Clinic, São Paulo, Brazil.
Marcos CochakGeneOne, São Paulo, Brazil.
Michele MigliavaccaGeneOne, São Paulo, Brazil.
Fernanda MilaneziGeneOne, São Paulo, Brazil.
Ana Cristina SousaGeneOne, São Paulo, Brazil.
Juliana SilvaGeneOne, São Paulo, Brazil.
Lígia VieiraGeneOne, São Paulo, Brazil.
Priscilla MonfrediniGeneOne, São Paulo, Brazil.
Ana Carolina PalumboGeneOne, São Paulo, Brazil.
Jonathas FernandesGeneOne, São Paulo, Brazil.
Eduardo PerroneDepartment of Clinical Genetics, Federal University of São Paulo, São Paulo, Brazil.
Universidade Federal de São Paulo · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Duplication of the distal 1q and 4p segments are both characterized by the presence of intellectual disability/neurodevelopmental delay and dysmorphisms. Here, we describe a male with a complex chromosome rearrangement (CCR) presenting with overlapping clinical findings between these 2 syndromes. In order to better characterize this CCR, classical karyotyping, FISH, and chromosomal microarray analysis were performed on material from the patient and his parents, which revealed an unbalanced karyotype with duplications at 1q41q43 and 4p15.2p14 in the proband. The rearrangements, which were derived from a maternal balanced karyotype, included an insertion of a segment from the long to the short arm of chromosome 1, a balanced translocation involving chromosomes 14 and 18, and an insertion of a segment from the short arm of chromosome 4 into the derived chromosome 14. This study aimed to better define the clinical history and prognosis of a patient with this rare category of chromosomal aberration. Our results suggest that the frequency of CCR in the general population may be underestimated; when balanced, they may not have a phenotypic effect. Moreover, they emphasize the need for cytogenetic techniques complementary to chromosomal microarray for proper genetic counseling.

Indexed as

Chromosome rearrangementDuplication 1qDuplication 4pFISHKaryotype

Identifiers

PMID34602959
PMCPMC8436616
OpenAlexW3183794406

What OpenQuestion holds

Textmetadata
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.