Evidence map›Paper›PMID 37859908›Full record

ArticleCureus2023

Li-Fraumeni Syndrome, A Rarity Among Rarities: A Case Report and Review of Literature.

Mariam Elremeli, Philip Idaewor, Noreen Rasheed, Abdalla Saad Abdalla Al-Zawi

Open access · diamondAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Cureus, 2023. 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, top 55% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

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 at 1 institution in 1 country.

Mariam ElremeliPaediatrics-Allergy/Immunology, Imperial College London, London, GBR.
Philip IdaeworHistopathology/Cellular Pathology, Mid and South Essex National Health Service (NHS) Foundation Trust, Basildon, GBR.
Noreen RasheedRadiology, Basildon and Thurrock University Hospital National Health Service (NHS) Foundation Trust, Basildon, GBR.
Abdalla Saad Abdalla Al-ZawiGeneral and Breast Surgery, Mid and South Essex National Health Service (NHS) Foundation Trust, Basildon, GBR.
National Health Service · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Li-Fraumeni syndrome (LFS) is a rare inherited cancer susceptibility disorder with a wide tumour spectrum, particularly in children and young adults. Patients with LFS have life-long cancer risk, and the most commonly encountered tumours include soft tissue sarcoma, breast cancer, brain tumours, osteosarcoma, leukaemia and adrenocortical carcinoma. LFS is associated with mutations in the tumour suppressor gene

Indexed as

brain pleomorphic xanthoastrocytomabreast cancerli-fraumeni syndrometp53 mutationupfront chemotherapy

Identifiers

PMID37859908
PMCPMC10583736
OpenAlexW4386829518

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.