Evidence map›Paper›PMID 38596967›Full record

ArticleHua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology2022

Non-syndromic familial congenital dental deficiency: two cases report.

Xue Chen, Yuangao Li

Open access · greenAbstract read
In one paragraph

Article in Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology, 2022. 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
0.1field-weighted citation impact, top 55% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

2 authors at 1 institution in 1 country.

Xue ChenDept. of Stomatology, Peking University Third Hospital, Beijing 100191, China.
Yuangao LiDept. of Stomatology, Peking University Third Hospital, Beijing 100191, China.
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital dental deficiency can lead to aesthetic and masticatory dysfunction, which have a great effect on the quality of life of patients. Genetic inheritance is the determining factor of congenital dental deficiency, which may follow the pattern of autosomal dominant, recessive, or sex chromosome inheritance. However, the specific genetic mechanisms are not clear. The prevalence of congenital absence of permanent teeth in the general population worldwide are not high, and familial oligodontia in clinically healthy patients is rare. This paper reported two cases of familial non-syndromic congenital teeth loss and included a review of literature referring to the etiology, clinical manifestations, and treatment of congenital dental deficiency.

Indexed as

congenital dental deficiencyetiologynon-syndromic

Identifiers

PMID38596967
PMCPMC9396427
OpenAlexW4394760246

What OpenQuestion holds

Textmetadata
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.