Evidence map›Paper›PMID 41246610›Full record

ArticleCureus2025

Vanishing Bones and Stubborn Joints: Unravelling the Enigma of Multicentric Osteolysis, Nodulosis, and Arthropathy Syndrome.

Rajat Kumar Sahu, Mukesh Maurya, Monalisha Sahoo, Urmila Dhakad, Puneet Kumar

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

5 authors.

Rajat Kumar SahuClinical Immunology and Rheumatology, King George's Medical University, Lucknow, IND.
Mukesh MauryaClinical Immunology and Rheumatology, King George's Medical University, Lucknow, IND.
Monalisha SahooResearch, King George's Medical University, Lucknow, IND.
Urmila DhakadClinical Immunology and Rheumatology, King George's Medical University, Lucknow, IND.
Puneet KumarClinical Immunology and Rheumatology, King George's Medical University, Lucknow, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multicentric osteolysis, nodulosis, and arthropathy (MONA) syndrome is a rare inherited skeletal disorder, transmitted in an autosomal recessive manner, marked by gradual bone loss, especially affecting the carpal and tarsal bones, and the presence of subcutaneous nodules. The condition results from mutations in the

Indexed as

and arthropathy (mona)arthritismmp 2monamulticentric osteolysisnodulosisosteolysis

Identifiers

PMID41246610
PMCPMC12614870

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.