Evidence map›Paper›PMID 38077305›Full record

ArticleJCEM case reports2023

A Novel Case of Concomitant PHEX and ALPL Mutation In a Family With Rickets.

Carmen Polanco Santos, Juana Cordero Garate, Leila Zeinab Khan

Open access · diamondAbstract readCase Reports
In one paragraph

Article in JCEM case reports, 2023. 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
0.2field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

3 authors at 2 institutions in 1 country.

Carmen Polanco SantosEndocrinology and Metabolism Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
Juana Cordero GarateJacobi Medical Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.ORCID https://orcid.org/0000-0002-3141-7517
Leila Zeinab KhanEndocrinology and Metabolism Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
Cleveland Clinic · USJacobi Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, no published cases report concomitant X-linked hypophosphatemia (XLH) and adult hypophosphatasia (HPP). Both diseases share clinical phenotypes that are almost indistinguishable. The correct diagnosis may be missed without a standardized laboratory and genetic testing approach. Pathogenic variants in the phosphate regulating endopeptidases homolog X-linked gene (

Indexed as

ALPLburosumab-twsahypophosphatasiahypophosphatemiaPHEXrickets

Identifiers

PMID38077305
PMCPMC10702626
OpenAlexW4389425555

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.