Evidence map›Paper›PMID 40703321›Full record

ArticleFrontiers in pediatrics2025

Comprehensive treatment approaches for skeletal deformities in hypophosphatasia: a case study of

Qiongjie Jiao, Guixia Ma, Qian Ni

Abstract read
In one paragraph

Article in Frontiers in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Qiongjie Jiao *Pediatric Respiratory Department, The Second Hospital of Lanzhou University, Lanzhou, China.
Guixia Ma *Pediatric Respiratory Department, The Second Hospital of Lanzhou University, Lanzhou, China.
Qian NiPediatric Respiratory Department, The Second Hospital of Lanzhou University, Lanzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study presents a case report of an 11-year-old boy with hypophosphatasia due to compound heterozygous

Indexed as

ALPL genetic variantscorrective chest wall deformityhypophosphatasiamultidisciplinary treatmentpediatric genetic diseaserespiratory dysfunction

Identifiers

PMID40703321
PMCPMC12283614

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.