Evidence map›Paper›PMID 39012089›Full record

ArticleJournal of clinical research in pediatric endocrinology2026

Autosomal Recessive Hypophosphatemic Rickets Type 2 Associated with a Novel

Han-Yi Lin, Ni-Chung Lee, Meng-Ju Melody Tsai, Ting-Ming Wang, Yi-Ching Tung

Abstract readCase Reports
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 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

5 authors.

Han-Yi LinNational Taiwan University Hospital Hsinchu Branch, Department of Pediatrics, Hsinchu, TaiwanORCID 0000-0001-5312-4056
Ni-Chung LeeNational Taiwan University Hospital, Department of Medical Genetics, Taipei, TaiwanORCID 0000-0002-5011-7499
Meng-Ju Melody TsaiNational Taiwan University Hospital Yunlin Branch, Department of Pediatrics, Douliu, Yunlin, TaiwanORCID 0009-0001-3528-2381
Ting-Ming WangNational Taiwan University Hospital, Department of Orthopedic Surgery, Taipei, TaiwanORCID 0000-0002-2263-5993
Yi-Ching TungNational Taiwan University Hospital, Department of Pediatrics, Taipei, TaiwanORCID 0000-0003-0466-3891

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autosomal recessive hypophosphatemic rickets (ARHR) type 2 (ARHR2) is a rare form of hypophosphatemic rickets (HR) caused by a variant of the gene encoding ectonucleotide pyrophosphatase/phosphodiesterase 1 (

Indexed as

Familial Hypophosphatemic RicketsMutationPhosphoric Diester HydrolasesPyrophosphatasesRickets, HypophosphatemicChild, PreschoolFemaleFibroblast Growth Factor-23HumansInfantTaiwanectonucleotide pyrophosphatase phosphodiesterase 1Fibroblast Growth Factor-23Phosphoric Diester HydrolasesPyrophosphatasesEncoding ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1)fibroblast growth factor 23 (FGF23)hypophosphatemic rickets

Identifiers

PMID39012089
PMCPMC13197086

What OpenQuestion holds

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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.