Evidence map›Paper›PMID 42081114›Full record

ArticleCalcified tissue international2026

Pre-eruptive Coronal Resorptions as a Clinical Feature of FAM83H-Related Amelogenesis Imperfecta: Insights from Two Brazilian Families.

Kemelly Karolliny Resende, Luanna de Sousa Amorim, Lilian Marly de Paula, André Ferreira Leite, Juliana Forte Mazzeu, Paulo Marcio Yamaguti, Ana Carolina Acevedo

Abstract readCase Reports
In one paragraph

Article in Calcified tissue international, 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. Editorial "Enamel" Issue.Calcified tissue international · 2026
    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

7 authors.

Kemelly Karolliny ResendeDepartment of Dentistry, Laboratory of Oral Histopathology, Faculty of Health Sciences, University of Brasilia, Brasilia, Brazil.
Luanna de Sousa AmorimDepartment of Dentistry, Laboratory of Oral Histopathology, Faculty of Health Sciences, University of Brasilia, Brasilia, Brazil.
Lilian Marly de PaulaDepartment of Dentistry, Laboratory of Oral Histopathology, Faculty of Health Sciences, University of Brasilia, Brasilia, Brazil.
André Ferreira LeiteOral Care Center for Inherited Diseases, University Hospital of Brasilia, Brasilia, Brazil.
Juliana Forte MazzeuLaboratory of Clinical Genetics, Faculty of Medicine, University of Brasília, Brasília, Brazil.
Paulo Marcio YamagutiDepartment of Dentistry, Laboratory of Oral Histopathology, Faculty of Health Sciences, University of Brasilia, Brasilia, Brazil.
Ana Carolina AcevedoDepartment of Dentistry, Laboratory of Oral Histopathology, Faculty of Health Sciences, University of Brasilia, Brasilia, Brazil. acevpoppe@gmail.com.ORCID http://orcid.org/0000-0001-7110-7110

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amelogenesis Imperfecta (AI) is a group of rare hereditary conditions characterized by quantitative and/or qualitative enamel defects affecting both primary and permanent dentitions. Among the more than 70 genes associated with AI, FAM83H is the only gene known to cause autosomal dominant hypocalcified AI (ADHCAI). Recent studies have shown that causative variants in FAM83H disrupt amelogenesis and may also affect dental follicle cells, potentially leading to tooth impaction in ADHCAI patients. Here, we report two unrelated Brazilian patients with ADHCAI who present a distinctive and severe phenotype characterized by delayed eruption, multiple impacted teeth, and pre-eruptive crown resorptions (PECR). Longitudinal radiographic analysis revealed multiple unerupted teeth with progressive PECR. Using whole-exome sequencing, we identified two nonsense heterozygous FAM83H causative variants (c.1055 C > A, p.Ser352*; c.1379G > A, p.Trp460*). Our findings represent the first report of FAM83H-related ADHCAI in Brazilian families and expand both the phenotypic spectrum and clinical severity associated with this gene. The presence of widespread PECR and adjacent bone alterations suggests that FAM83H dysfunction may affect not only enamel formation but also tooth eruption pathways and local tooth-bone interactions. This study highlights the importance of early diagnosis, individualized radiographic follow-up, and genetic testing to guide counselling and clinical management of affected individuals.

Indexed as

Amelogenesis ImperfectaProteinsTooth ResorptionAdolescentBrazilExome SequencingFemaleHumansMalePedigreePhenotypeFAM83H protein, humanProteinsAmelogenesis ImperfectaFAM83HPre-eruptive crown resorptionTooth impactionWhole-exome sequencing

Identifiers

PMID42081114
PMCPMC13139228

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LicenceCC BY
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Registered trials

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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.