Evidence map›Paper›PMID 40998536›Full record

ArticleBMJ case reports2025

Melkersson-Rosenthal syndrome: recurrent facial swelling and food refusal.

Xanthea Dewez, Nitaa Eapen, Hafsah Brown, Jye Gard

Abstract readCase Reports
In one paragraph

Article in BMJ case reports, 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

4 authors.

Xanthea DewezGeneral Medicine, Royal Children's Hospital Melbourne Department of General Medicine, Parkville, Victoria, Australia xantheadewez1@gmail.com.
Nitaa EapenGeneral Medicine, Royal Children's Hospital Melbourne Department of General Medicine, Parkville, Victoria, Australia.
Hafsah BrownGeneral Medicine, Royal Children's Hospital Melbourne Department of General Medicine, Parkville, Victoria, Australia.
Jye GardGeneral Medicine, Royal Children's Hospital Melbourne Department of General Medicine, Parkville, Victoria, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with Melkersson-Rosenthal syndrome (MRS) experience prolonged periods of functional impairment due to partial or complete facial paralysis and orofacial oedema that interferes with their ability to eat, drink, taste, express emotions and speak. Younger children with MRS are at high risk of nasogastric feeding dependency and additional chronic feeding challenges due to the cumulative impacts of disease flares during the period when feeding skills and interest in foods are first developed. We present a case of a boy in early childhood who presented multiple times over a 4 month period with predominant symptoms of recurrent unilateral facial swelling and significantly reduced oral intake and who was eventually diagnosed with MRS.

Indexed as

EdemaFacial ParalysisMelkersson-Rosenthal SyndromeChild, PreschoolFaceHumansMaleRecurrenceChildhood nutrition (paediatrics)Congenital disordersInfant nutrition (including breastfeeding)

Identifiers

PMID40998536
PMCPMC12481182

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.