Evidence map›Paper›PMID 39252496›Full record

ArticleDevelopmental medicine and child neurology2025

Long-term outcomes in children with riboflavin transporter deficiency and surveillance recommendations.

Jack R Fennessy, Kayla M D Cornett, Gabrielle A Donlevy, Marnee J Mckay, Joshua Burns, Manoj P Menezes

Abstract read
In one paragraph

Article in Developmental medicine and child neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
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

6 authors.

Jack R FennessyFaculty of Medicine and Health, University of Sydney School of Health Sciences, Sydney, New South Wales, Australia.ORCID 0000-0002-7985-7837
Kayla M D CornettFaculty of Medicine and Health, University of Sydney School of Health Sciences, Sydney, New South Wales, Australia.ORCID 0000-0002-9863-1040
Gabrielle A DonlevyFaculty of Medicine and Health, University of Sydney School of Health Sciences, Sydney, New South Wales, Australia.ORCID 0000-0002-4708-5879
Marnee J MckayFaculty of Medicine and Health, University of Sydney School of Health Sciences, Sydney, New South Wales, Australia.ORCID 0000-0002-8126-3579
Joshua BurnsFaculty of Medicine and Health, University of Sydney School of Health Sciences, Sydney, New South Wales, Australia.
Manoj P MenezesChildren's Hospital at Westmead Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.ORCID 0000-0003-3160-6112

Funding

trainingU54NS065712 · NINDS · WAYNE STATE UNIVERSITY · PI SHY, MICHAEL E. · 2009 to 2023
$19.6M
Accelerate Clinical Trials in CMT (ACTCMT) StudyU01NS109403 · NINDS · UNIVERSITY OF ROCHESTER · PI HERRMANN, DAVID N · 2019 to 2023
$6.4M
Cure RTD FoundationNINDS NIH HHS U01 NS109403NINDS NIH HHS U54 NS065712
6 · The paper itself

Abstract

The aim of this longitudinal case series was to describe long-term functional outcome in a group of individuals with riboflavin transporter deficiency (RTD) treated with high-dose oral riboflavin. Data were collected between 2012 to 2022. Eleven individuals with RTD were assessed at 12-month intervals for monitoring of disease progression. Patients had commenced high-dose oral riboflavin from the time of genetic diagnosis. Individuals for whom riboflavin supplementation was initiated early after disease onset had better outcomes compared to those in whom diagnosis was delayed. Despite ongoing riboflavin supplementation, the Charcot-Marie-Tooth disease Pediatric Scale (CMTPedS) total score and the subitems of balance and the 6-Minute Walk Test distance as well as respiratory function worsened, while grip strength improved. There was evidence of improvement in hearing loss and optic atrophy limited to the first 12 months of treatment. While treatment with riboflavin slowed disease progression, patients were left with residual disability. To track disease progression and response to riboflavin supplementation over time, we recommend using the RTD Pediatric Scale and provide a list of clinical measures for regular surveillance of children with RTD.

Indexed as

Hearing Loss, SensorineuralMembrane Transport ProteinsRiboflavinAdolescentBulbar Palsy, ProgressiveChildChild, PreschoolDisease ProgressionFemaleHumansLongitudinal StudiesMaleTreatment OutcomeMembrane Transport ProteinsRiboflavin

Identifiers

PMID39252496
PMCPMC11794669

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Registered trials

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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.