Evidence map›Paper›PMID 41179007›Full record

ArticleCureus2025

A Phenotypically Normal Homozygous Balanced Reciprocal Translocation Carrier: Report of an Extremely Rare Genetic Occurrence.

Mitila Thirupathy, Mitesh Shetty, Priya Prakash

Abstract readCase Reports
In one paragraph

Article in Cureus, 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

3 authors.

Mitila ThirupathyMedical Genetics, Manipal Hospital, Bengaluru, IND.
Mitesh ShettyMedical Genetics, Manipal Hospital, Bengaluru, IND.
Priya PrakashMedical Genetics, Manipal Hospital, Bengaluru, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Balanced reciprocal translocations (BRT) are relatively common structural chromosomal abnormalities and are typically observed in the heterozygous state. Homozygosity for reciprocal translocations is exceedingly rare, with most documented cases presenting with severe congenital anomalies or developmental delays. To the best of our knowledge, this is the second reported case of a phenotypically normal homozygous BRT carrier born from a natural conception. A 31-year-old female with primary infertility was found to be homozygous for the balanced reciprocal translocation t(11;22)(q23.3;q11.2) during assessment after a failed cycle of in vitro fertilization. Although homozygosity for such translocations can theoretically lead to meiotic errors, gene disruption, or recessive disorders, the proband exhibited a normal phenotype, likely owing to the completely balanced nature of the translocation, making this an exceptionally rare occurrence, challenging assumptions about the consequences of homozygous translocations, and highlighting the need for further research into the specific breakpoint regions.

Indexed as

balanced reciprocal translocationhomozygousinfertilitypgt-srsegregation patterns

Identifiers

PMID41179007
PMCPMC12576047

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.