Evidence map›Paper›PMID 33251707›Full record

ArticleAmerican journal of medical genetics. Part A2021

Heterozygous recurrent HNF4A variant p.Arg85Trp causes Fanconi renotubular syndrome 4 with maturity onset diabetes of the young, an autosomal dominant phenocopy of Fanconi Bickel syndrome with colobomas.

Sarah E Sheppard, Brett Barrett, Colleen Muraresku, Heather McKnight, Diva D De Leon, Katherine Lord, Rebecca Ganetzky

Open access · greenAbstract readCase Reports
In one paragraph

Article in American journal of medical genetics. Part A, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Genes · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Sarah E SheppardDivision of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.ORCID 0000-0003-3480-8123
Brett BarrettDivision of Endocrinology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Colleen MurareskuDivision of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Heather McKnightDivision of Endocrinology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Diva D De LeonDepartment of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID 0000-0003-1225-8087
Katherine LordDepartment of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Rebecca GanetzkyDepartment of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID 0000-0001-6238-8109
Children's Hospital of Philadelphia · US

Funding

NRSA Training CoreTL1TR001880 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI MEAGHER, EMMA ANNE · 2016 to 2025
$10.0M
Characterizing Cell and Zebrafish Models of Mitochondrial Complex V DeficiencyK08DK113250 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI GANETZKY, REBECCA · 2017 to 2021
$892k
NCATS NIH HHS TL1 TR001880NIDDK NIH HHS K08 DK113250NIDDK NIH HHS K08-DK113250
6 · The paper itself

Abstract

Heterozygous pathogenic variants in HNF4A cause hyperinsulinism, maturity onset diabetes of the young type 1, and more rarely Fanconi renotubular syndrome. Specifically, the recurrent missense pathogenic variant c.253C>T (p.Arg85Trp) has been associated with a syndromic form of hyperinsulinism with additional features of macrosomia, renal tubular nephropathy, hypophosphatemic rickets, and liver involvement. We present an affected mother, who had been previously diagnosed clinically with the autosomal recessive Fanconi Bickel Syndrome, and her affected son. The son's presentation expands the clinical phenotype to include multiple congenital anomalies, including penile chordee with hypospadias and coloboma. This specific pathogenic variant should be considered in the differential diagnosis of Fanconi Bickel Syndrome when genetics are negative or the family history is suggestive of autosomal dominant inheritance. The inclusion of hyperinsulinism and maturity onset of the diabetes of the young changes the management of this syndrome and the recurrence risk is distinct. Additionally, this family also emphasizes the importance of genetic confirmation of clinical diagnoses, especially in adults who grew up in the premolecular era that are now coming to childbearing age. Finally, the expansion of the phenotype to include multiple congenital anomalies suggests that the full spectrum of HNF4A is likely unknown.

Indexed as

Genetic Predisposition to DiseaseAge of OnsetColobomaDiabetes MellitusFamilial Hypophosphatemic RicketsFanconi SyndromeFemaleFetal MacrosomiaHepatocyte Nuclear Factor 4HeterozygoteHumansMaleMutation, MissensePedigreePregnancyHepatocyte Nuclear Factor 4HNF4A protein, humanFanconi renotubular syndromeHNF4Ahyperinsulinismmaturity onset diabetes of the young (MODY)

Identifiers

PMID33251707
PMCPMC8132289
OpenAlexW3107649838

What OpenQuestion holds

Textmetadata
LicenceTDM
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.