Evidence map›Paper›PMID 32776440›Full record

ArticleAmerican journal of medical genetics. Part A2020

Whole genome sequence analysis identifies a PAX2 mutation to establish a correct diagnosis for a syndromic form of hyperuricemia.

Mark Stevenson, Alistair T Pagnamenta, Silvia Reichart, Charlotte Philpott, Kate E Lines, OxClinWGS, Caroline M Gorvin, Karl Lhotta, Jenny C Taylor, Rajesh V Thakker

Open access · hybridAbstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Variable Phenotypic Expression ofMedicina (Kaunas, Lithuania) · 2025
    Article
  3. Article
  4. Article
  5. 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

10 authors at 4 institutions in 2 countries.

Mark StevensonOxford Centre for Diabetes, Endocrinology & Metabolism (OCDEM), Churchill Hospital, University of Oxford, Oxford, UK.ORCID https://orcid.org/0000-0001-8616-0205
Alistair T PagnamentaOxford BRC, WCHG, University of Oxford, Oxford, UK.
Silvia ReichartDepartment of Ophthalmology, Academic Teaching Hospital, Feldkirch, Austria.
Charlotte PhilpottOxford Centre for Diabetes, Endocrinology & Metabolism (OCDEM), Churchill Hospital, University of Oxford, Oxford, UK.
Kate E LinesOxford Centre for Diabetes, Endocrinology & Metabolism (OCDEM), Churchill Hospital, University of Oxford, Oxford, UK.
OxClinWGS
Caroline M GorvinOxford Centre for Diabetes, Endocrinology & Metabolism (OCDEM), Churchill Hospital, University of Oxford, Oxford, UK.
Karl LhottaDepartment of Internal Medicine III (Nephrology and Dialysis), Academic Teaching Hospital, Feldkirch, Austria.
Jenny C TaylorOxford BRC, WCHG, University of Oxford, Oxford, UK.
Rajesh V ThakkerOxford Centre for Diabetes, Endocrinology & Metabolism (OCDEM), Churchill Hospital, University of Oxford, Oxford, UK.
Churchill Hospital · GBLandeskrankenhaus Feldkirch · ATUniversity of Oxford · GBOxford Centre for Diabetes, Endocrinology and Metabolism · GB

Funding

Medical Research Council G1000467Medical Research Council G9825289Wellcome Trust 100127Wellcome Trust 106995Wellcome Trust Senior Clinical Investigator Award
6 · The paper itself

Abstract

Hereditary hyperuricemia may occur as part of a syndromic disorder or as an isolated nonsyndromic disease, and over 20 causative genes have been identified. Here, we report the use of whole genome sequencing (WGS) to establish a diagnosis in a family in which individuals were affected with gout, hyperuricemia associated with reduced fractional excretion of uric acid, chronic kidney disease (CKD), and secondary hyperparathyroidism, that are consistent with familial juvenile hyperuricemic nephropathy (FJHN). However, single gene testing had not detected mutations in the uromodulin (UMOD) or renin (REN) genes, which cause approximately 30-90% of FJHN. WGS was therefore undertaken, and this identified a heterozygous c.226G>C (p.Gly76Arg) missense variant in the paired box gene 2 (PAX2) gene, which co-segregated with renal tubulopathy in the family. PAX2 mutations are associated with renal coloboma syndrome (RCS), which is characterized by abnormalities in renal structure and function, and anomalies of the optic nerve. Ophthalmological examination in two adult brothers affected with hyperuricemia, gout, and CKD revealed the presence of optic disc pits, consistent with optic nerve coloboma, thereby revising the diagnosis from FJHN to RCS. Thus, our results demonstrate the utility of WGS analysis in establishing the correct diagnosis in disorders with multiple etiologies.

Indexed as

MutationAdultCreatinineDNA Mutational AnalysisFemaleHeterozygoteHumansHyperparathyroidism, SecondaryHyperuricemiaMaleMiddle AgedMutation, MissensePAX2 Transcription FactorPedigreeRenal Insufficiency, ChronicReninCreatininePAX2 protein, humanPAX2 Transcription FactorReninUric AcidUromodulinADTKDCKDoptic disc pitspapillorenal syndromeRCS

Identifiers

PMID32776440
PMCPMC7611017
OpenAlexW3048663104

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.