Evidence map›Paper›PMID 38576635›Full record

ArticleCureus2024

18p Deletion Syndrome With a 45, XY, t (14;18) (p11.1; p11.1), Karyotype.

Baraah Ashgan, Abdulmoein Al-Agha, Yara Alhamdani, Mohamed Abdelmaksoud Shazly

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Cureus, 2024. 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

4 authors.

Baraah AshganPediatrics, Faculty of Medicine, King Abdulaziz University Hospital, Jeddah, SAU.
Abdulmoein Al-AghaPediatric Endocrinology, Faculty of Medicine, King Abdulaziz University Hospital, Jeddah, SAU.
Yara AlhamdaniPediatrics, Faculty of Medicine, King Abdulaziz University Hospital, Jeddah, SAU.
Mohamed Abdelmaksoud ShazlyPediatric Endocrinology, Faculty of Medicine, King Abdulaziz University Hospital, Jeddah, SAU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monosomy 18p deletion syndrome is a rare genetic disorder. We present an uncommon case of 18p deletion syndrome originating from a unique translocation between chromosomes 14 and 18 in an 11-year-old Saudi male, manifesting various clinical features. This case highlights the importance of understanding the genotype-phenotype correlations of 18p deletion syndrome to aid in the early recognition of the syndrome for its effective diagnosis and management.

Indexed as

18p deletion syndromedysmorphic featuregrowth hormone deficiencyshort staturetranslocation

Identifiers

PMID38576635
PMCPMC10993083

What OpenQuestion holds

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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.