Evidence map›Paper›PMID 41459630›Full record

ArticleClinical genetics2026

Retinal Pigment Epitheliopathy due to Sub-Optimal Recycling of Vitamin A (RESORVA): A Novel RDH11 -Related Phenotype.

Kirk A J Stephenson, Zhuo Shao, Anupreet Tumber, Erika Tavares, Kashif Ahmed, Edward J Higginbotham, Christian R Marshall, Jason T Maynes, Ammaji Rajala, Raju V S Rajala and 2 more

Abstract readCase Reports
In one paragraph

Article in Clinical genetics, 2026. 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

12 authors.

Kirk A J StephensonOphthalmology and Vision Sciences, The Hospital for Sick Children (HSC), Toronto, Ontario, Canada.ORCID 0000-0002-7462-7725
Zhuo ShaoGenetics Program, North York General Hospital, University of Toronto, Toronto, Ontario, Canada.
Anupreet TumberOphthalmology and Vision Sciences, The Hospital for Sick Children (HSC), Toronto, Ontario, Canada.
Erika TavaresGenetics and Genome Biology, The Hospital for Sick Children (HSC), Toronto, Ontario, Canada.
Kashif AhmedGenetics and Genome Biology, The Hospital for Sick Children (HSC), Toronto, Ontario, Canada.
Edward J HigginbothamDivision of Genome Diagnostics, Department of Pediatric Laboratory Medicine, The Hospital for Sick Children (HSC), Toronto, Ontario, Canada.
Christian R MarshallDivision of Genome Diagnostics, Department of Pediatric Laboratory Medicine, The Hospital for Sick Children (HSC), Toronto, Ontario, Canada.
Jason T MaynesAnesthesia and Pain Medicine and Program in Molecular Medicine, The Hospital for Sick Children (HSC), Toronto, Ontario, Canada.
Ammaji RajalaDepartment of Ophthalmology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.
Raju V S RajalaDepartment of Ophthalmology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.
Elise HéonOphthalmology and Vision Sciences, The Hospital for Sick Children (HSC), Toronto, Ontario, Canada.
Ajoy VincentOphthalmology and Vision Sciences, The Hospital for Sick Children (HSC), Toronto, Ontario, Canada.

Funding

Foundation Fighting Blindness CD-CMM-0224-0873-HSC
6 · The paper itself

Abstract

Retinol dehydrogenases (RDHs) catalyze multiple steps in the visual cycle to regenerate 11-cis-retinal, a critical component in rod phototransduction. The structural homology between RDHs enables functional redundancy; yet Mendelian disorders are linked to RDHs. Variants in RDH12 and RDH5 cause non-syndromic inherited retinal dystrophy (IRD), whilst variants in RDH11 cause syndromic IRD. RDH11 is a minor isoenzyme catalyzing two reactions: (i) reduction of all-trans-retinal in rod photoreceptors alongside RDH12 and RDH8, and (ii) oxidation of 11-cis-retinol in the retinal pigment epithelium (RPE) alongside RDH5 and RDH10. Prior cases with RDH11 demonstrated a generalized photoreceptor dystrophy, similar to RDH12-retinopathy. We describe a visually asymptomatic 7-year-old boy carrying a homozygous null variant in RDH11 [NM_016026.4:c.216C>A:p.(Cys72*)] with autism, dysmorphic features, oligodontia, microcephaly and a novel IRD. This retinopathy consisted of yellow deposits and hyperpigmentation within the RPE with absent autofluorescence and a normal electroretinogram implying sub-optimal oxidation of 11-cis-retinol. These features are reminiscent of RDH5-retinopathy but milder. We termed this phenotype Retinal pigment Epitheliopathy due to Sub-Optimal Recycling of Vitamin A (RESORVA). We propose that the divergence in retinal phenotypes among RDH11 cases is likely due to variant-specific protein effects on paralogous gene functioning, such as differences in activation of transcriptional adaptation.

Indexed as

Alcohol OxidoreductasesRetinal DystrophiesRetinal Pigment EpitheliumVitamin AChildHomozygoteHumansMaleMutationPhenotypeAlcohol OxidoreductasesVitamin Aautism spectrum disordermicrocephalyRDH11retinaldehyderetinal dystrophiesvitamin A

Identifiers

PMID41459630
PMCPMC13066773

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.