Evidence map›Paper›PMID 35418376›Full record

ArticleBMJ case reports2022

Dental phenotype in an adolescent with osteogenesis imperfecta type XII.

Joanna Yuet-Ling Tung, Jeni Lai-In Ho, Ricky Wong, Siu-Chung Fung

Open access · hybridAbstract readCase Reports
In one paragraph

Article in BMJ case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Preserved bone mineral density in autosomal dominant SP7-related osteogenesis imperfecta: a case report of the p.Glu340Ala variant.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2026
    Article
  3. Update on the Genetics of Osteogenesis Imperfecta.Calcified tissue international · 2024
    Review
  4. Regulation of Skeletal Development and Maintenance by Runx2 and Sp7.International journal of molecular sciences · 2024
    Review
  5. A homozygousJBMR plus · 2024
    Article
  6. Review
  7. SP7: from Bone Development to Skeletal Disease.Current osteoporosis reports · 2023
    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

4 authors at 1 institution in 1 country.

Joanna Yuet-Ling TungDepartment of Paediatrics and Adolescent Medicine, Hong Kong Children's Hospital, Hong Kong, Hong Kong tungylj@yahoo.com.hk.ORCID http://orcid.org/0000-0001-7897-716X
Jeni Lai-In HoDepartment of Dentistry and Maxillofacial Surgery, Hong Kong Children's Hospital, Hong Kong, Hong Kong.
Ricky WongDepartment of Dentistry and Maxillofacial Surgery, Hong Kong Children's Hospital, Hong Kong, Hong Kong.
Siu-Chung FungDepartment of Dentistry and Maxillofacial Surgery, Hong Kong Children's Hospital, Hong Kong, Hong Kong.
Duchess of Kent Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutation in SP7, encoding the osteoblast-specific transcription factor SP7 (also known as osterix), has been described to cause osteogenesis imperfecta (OI) type XII. However, the exact dental phenotype has not been well described. We report the detailed dental manifestation of a boy known to have OI type XII, presented with impacted dentition, necessitating combined oral and maxillofacial surgical and orthodontic treatment. This case also highlighted the need of multidisciplinary team assessment in this group of children.

Indexed as

Osteogenesis ImperfectaAdolescentHumansMutationOsteoblastsPhenotypeDentistry and oral medicineOsteoporosisPaediatrics (drugs and medicines)

Identifiers

PMID35418376
PMCPMC9013958
OpenAlexW4223966384

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.