Evidence map›Paper›PMID 42667116›Full record

ArticleSpecial care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry

Orthodontic and Craniofacial Skeletal Alterations in Individuals With Thalassemia: A Scoping Review.

Larissa Conrado da Silva, Diego Belmiro do Nascimento Santos, José Alcides Almeida de Arruda, Lucas Guimarães Abreu, Victor Zanetti Drumond, Thalyta Cristina Souza da Silva Cruz, Matilde da Cunha Gonçalves Nojima, Bruno Augusto Benevenuto de Andrade, Jefferson R Tenório

Abstract readScoping Review
In one paragraph

Article in Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry. 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

9 authors.

Larissa Conrado da SilvaDepartment of Oral Diagnosis and Pathology, School of Dentistry, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Diego Belmiro do Nascimento SantosDepartment of Oral Diagnosis and Pathology, School of Dentistry, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
José Alcides Almeida de ArrudaDepartment of Oral Diagnosis and Pathology, School of Dentistry, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0002-6599-3950
Lucas Guimarães AbreuDepartment of Child and Adolescent Oral Health, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID https://orcid.org/0000-0003-2258-8071
Victor Zanetti DrumondDepartment of Oral Surgery, Pathology, and Clinical Dentistry, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID https://orcid.org/0000-0002-5270-3950
Thalyta Cristina Souza da Silva CruzDepartment of Oral Diagnosis and Pathology, School of Dentistry, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Matilde da Cunha Gonçalves NojimaDepartment of Pediatric Dentistry and Orthodontics, School of Dentistry, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Bruno Augusto Benevenuto de AndradeDepartment of Oral Diagnosis and Pathology, School of Dentistry, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0002-3259-606X
Jefferson R TenórioDepartment of Oral Diagnosis and Pathology, School of Dentistry, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0002-6986-9148

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThalassemia is a well-recognized hereditary blood disorder with systemic complications. However, its craniofacial and orthodontic alterations remain incompletely characterized. Current evidence is fragmented, and no comprehensive synthesis has been published hitherto.

aimsTo map and synthesize craniofacial and orthodontic alterations in individuals with thalassemia by identifying morphological patterns and associated clinical factors.

methodsThis scoping review included cross-sectional studies, cohort studies, and clinical trials retrieved from four databases and gray literature. Data were analyzed descriptively.

resultsTwenty-six studies (comprising 2,353 participants) published between 1964 and 2025 were included. Common findings included a Class II skeletal pattern, mandibular retrusion, maxillary protrusion, increased lower facial height, and thalassemic facies. Orthodontic anomalies included Class II malocclusion, anterior open bite, crowding, incisor protrusion, and transverse constriction of the arches (narrow skeletal arches). Greater severity was associated with chronic anemia, splenectomy, and delayed transfusion. Only one study evaluated functional appliance therapy, demonstrating improved mandibular advancement and facial esthetics.

conclusionThalassemia is associated with clinically relevant dentoskeletal alterations that affect function and esthetics. Early orthodontic evaluation and timely interceptive treatment should be prioritized, as they may attenuate deformity progression and improve craniofacial development, reducing the future need for complex orthognathic surgery.

Indexed as

Craniofacial AbnormalitiesMalocclusionThalassemiaHumansmaxillofacial abnormalitiesorofacial deformitiesorthodonticsthalassemia

Identifiers

PMID42667116
PMCPMC13525490

What OpenQuestion holds

Textmetadata
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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.