Evidence map›Paper›PMID 41200573›Full record

ArticleBalkan journal of medical genetics : BJMG2025

Partial Trisomy of Chromosome 9 Inherited by Adjacent Segregation 2 of a Balanced Reciprocal Translocation in the Mother: Rare Mechanism in Chromosomal Abnormalities.

K Zerrouki, F E Aouni, F Smaili, J Ahmidi, S Meziane, K Ahmidouch, M Tajir

Abstract readCase Reports
In one paragraph

Article in Balkan journal of medical genetics : BJMG, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

K ZerroukiLaboratory of epidemiology, clinical research and public health, Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco.
F E AouniLaboratory of epidemiology, clinical research and public health, Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco.
F SmailiLaboratory of epidemiology, clinical research and public health, Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco.
J AhmidiLaboratory of epidemiology, clinical research and public health, Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco.
S MezianeLaboratory of epidemiology, clinical research and public health, Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco.
K AhmidouchLaboratory of epidemiology, clinical research and public health, Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco.
M TajirLaboratory of epidemiology, clinical research and public health, Faculty of Medicine and Pharmacy, Mohammed Premier University, Oujda, Morocco.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Reciprocal translocations are one of the most common structural chromosomal rearrangements in humans, they are due to the exchange of chromosome material between two nonhomologous chromosomes.If a person carries a balanced reciprocal translocation, meiosis may produce normal gametes, as well as gametes with either balanced or unbalanced abnormalities, depending on the segregation pattern during gametogenesis. All types of segregations can occur, although with different percentages. The adjacent-2 segregation is the less common one and it often leads to non-viable products in many species. Case presentation: We report a case of an 18 months-old female patient, who was referred to the medical genetics' consultation for psychomotor retardation and facial dysmorphism. A postnatal constitutional karyotype was performed in our laboratory on a peripheral blood sample followed by a parental karyotype. The results revealed an additional derivative chromosome 9 in the patient resulting from an adjacent-2 segregation in the mother. Conclusion: This observation highlights the possible occurrence of rare mechanisms of segregation during meiosis in families with a reciprocal translocation. Investigating these events is crucial for both diagnosis and genetic counseling.

Indexed as

adjacent-2 segregationcongenital malformationsReciprocal translocationssegregation mechanisms

Identifiers

PMID41200573
PMCPMC12588064

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.