Evidence map›Paper›PMID 42465702›Full record

ArticleCureus2026

Benefit of Salbutamol for the Treatment of Neuromuscular Junction Dysfunction in Patients With Purine-Rich Element Binding Protein A (PURA) Syndrome.

Maggie L Yau, Cara Beck, Eva L Fung, Eppie M Yiu, Chiara Tewierik, Chun-Him Leung, Hon-Ming Cheung, Karen K Yam, Ka-Nam Wong, Thomas S O'Neill and 2 more

Abstract readCase Reports
In one paragraph

Article in Cureus, 2026. 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

12 authors.

Maggie L YauPaediatrics, The Chinese University of Hong Kong, Sha Tin, HKG.
Cara BeckVictorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, AUS.
Eva L FungPaediatrics, The Chinese University of Hong Kong, Sha Tin, HKG.
Eppie M YiuNeurology, The Royal Children's Hospital, Melbourne, AUS.
Chiara TewierikPhysiotherapy, The Royal Children's Hospital, Melbourne, AUS.
Chun-Him LeungPhysiotherapy, Prince of Wales Hospital, Sha Tin, HKG.
Hon-Ming CheungPaediatrics, The Chinese University of Hong Kong, Sha Tin, HKG.
Karen K YamPaediatrics, The Chinese University of Hong Kong, Sha Tin, HKG.
Ka-Nam WongPaediatrics, The Chinese University of Hong Kong, Sha Tin, HKG.
Thomas S O'NeillNeurology, The Royal Children's Hospital, Melbourne, AUS.
Katherine B HowellNeurology, The Royal Children's Hospital, Melbourne, AUS.
Shuk-Ching ChongPaediatrics, The Chinese University of Hong Kong, Sha Tin, HKG.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purine-rich element-binding protein A (PURA) syndrome is a rare neurodevelopmental disorder caused by pathogenic variants in the PURA gene and is characterized by neonatal hypotonia, feeding difficulty, respiratory dysregulation, and severe developmental impairment. The PURA gene has recently been identified as a cause of congenital myasthenic syndrome. We report two unrelated infants with genetically confirmed PURA syndrome who were treated with neuromuscular junction-directed therapy and reviewed three additional published cases. All five patients had neonatal hypotonia and apnea or respiratory failure requiring respiratory support. Pyridostigmine was used in four of the five infants included with heterogeneous response, while salbutamol, used in three patients, was associated with clinical benefit in all. These findings suggest that neuromuscular junction dysfunction may contribute to the respiratory and motor phenotype in patients with PURA syndrome. Early consideration of salbutamol, with careful monitoring and objective outcome measurement, may help stabilize severe infantile respiratory failure and improve motor function.

Indexed as

congenital myasthenia syndromegenetic syndromesneuromuscular diseasespura syndrometreatment choices

Identifiers

PMID42465702
PMCPMC13375090

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.