Evidence map›Paper›PMID 42787692›Full record

ArticleCureus2026

SLC52A3-Related Riboflavin Transporter Deficiency in Two Saudi Siblings: A Case Report.

Fadi Busaleh, Nabil Almajhad, Ola H Alabbad, Dalal M Alshehri, Reham R Alhassan, Ghaliah Y Alhejji, Mariyyah A Al Jamea, Amnah F Alomran, Shomos H Aldulaim, Fatema M Almohammad Saleh and 1 more

Abstract readCase Reports
PubMed Full text at PMC Publisher
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

11 authors.

Fadi BusalehPediatrics/Pediatric Neurology, Maternity and Children's Hospital, Al-Ahsa, SAU.
Nabil AlmajhadPediatrics/Pediatric Neurology, Maternity and Children's Hospital, Al-Ahsa, SAU.
Ola H AlabbadMedicine, College of Medicine, King Faisal University, Al-Ahsa, SAU.
Dalal M AlshehriMedicine, King Faisal University, Dammam, SAU.
Reham R AlhassanPediatrics, King Faisal University, Al-Ahsa, SAU.
Ghaliah Y AlhejjiMedicine, College of Medicine, King Faisal University, Al-Ahsa, SAU.
Mariyyah A Al JameaMedicine, College of Medicine, King Faisal University, Al-Ahsa, SAU.
Amnah F AlomranMedicine, College of Medicine, King Faisal University, Al-Ahsa, SAU.
Shomos H AldulaimMedicine, College of Medicine, King Faisal University, Al-Ahsa, SAU.
Fatema M Almohammad SalehMedicine, King Faisal University, Al-Ahsa, SAU.
Anwar F AlqadeepMedicine, College of Medicine, King Faisal University, Al-Ahsa, SAU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brown-Vialetto-Van Laere syndrome (BVVLS), or riboflavin transporter deficiency (RTD), is a rare but treatable neurodegenerative disorder caused by pathogenic variants in the riboflavin transporter genes. We report the cases of two siblings with genetically confirmed

Indexed as

brown-vialetto-van laere syndromebulbar palsydevelopmental regressionsensorineural (sn) hearing lossslc52a3

Identifiers

PMID42787692
PMCPMC13601941

What OpenQuestion holds

Textmetadata
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.