Evidence map›Paper›PMID 41368056›Full record

ArticleClinical case reports2025

Myasthenia Gravis in a Child With Schimke Immuno-Osseous Dysplasia: A Case Report.

Mohamed S Al Riyami, Intisar Al Alawi, Maisa Al Riyami, Badria Al Gaithi, Suliman Al Saidi, Ibtisam Al Shuaili, Naifain Al Kalbani, Nabil Al Maki

Abstract read
In one paragraph

Article in Clinical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Mohamed S Al RiyamiPediatric Nephrology Unit, Department of Child Health Royal Hospital Muscat Oman.
Intisar Al AlawiNational Genetic Center, Ministry of Health Muscat Oman.
Maisa Al RiyamiPediatric Nephrology Unit, Department of Child Health Royal Hospital Muscat Oman.ORCID https://orcid.org/0000-0003-3698-5609
Badria Al GaithiPediatric Nephrology Unit, Department of Child Health Royal Hospital Muscat Oman.
Suliman Al SaidiPediatric Nephrology Unit, Department of Child Health Royal Hospital Muscat Oman.
Ibtisam Al ShuailiDepartment of Radiology Royal Hospital Muscat Oman.
Naifain Al KalbaniPediatric Nephrology Unit, Department of Child Health Royal Hospital Muscat Oman.
Nabil Al MakiPediatric Neurology Unit, Department of Child Health Royal Hospital Muscat Oman.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a rare association between Schimke immune-osseous dysplasia and myasthenia gravis. Clinicians should be aware of potential autoimmune neuromuscular complications in SIOD, as early recognition and tailored immunosuppression may improve prognosis.

Indexed as

autoimmunityend‐stage renal failuremyasthenia gravis SMARCAL1 gene mutationSchimke immune‐osseous dysplasia (SIOD)steroid‐resistant nephrotic syndrome

Identifiers

PMID41368056
PMCPMC12682587

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.