Evidence map›Paper›PMID 42578177›Full record

ArticleAnnals of maxillofacial surgery

Validation of Thymocyte Selection-associated High-mobility Group Box-3 Gene Mutation and Risk Identification in Non-syndromic Cleft Lip and Palate Deformities in Malay Patients - A Retrospective Study.

Izzeddin Jameel Abualjubain, Nurul Syazana Binti Mohamad Shah, Wan Azman Wan Sulaiman, Noor Areefa Ameera Mohd Ma'amor, Heba Mohammed Arafat

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Article in Annals of maxillofacial surgery. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Izzeddin Jameel AbualjubainReconstructive Sciences Unit, School of Medical Sciences, Health Campus, Universiti Sains Malaysia.
Nurul Syazana Binti Mohamad ShahReconstructive Sciences Unit, School of Medical Sciences, Health Campus, Universiti Sains Malaysia.
Wan Azman Wan SulaimanReconstructive Sciences Unit, School of Medical Sciences, Health Campus, Universiti Sains Malaysia.
Noor Areefa Ameera Mohd Ma'amorReconstructive Sciences Unit, School of Medical Sciences, Health Campus, Universiti Sains Malaysia.
Heba Mohammed ArafatDepartment of Chemical Pathology, School of Medical Sciences, Health Campus, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Non-syndromic cleft lip and/or palate (NSCL/P) is a common congenital deformity, influenced by both genetic and environmental factors. The thymocyte selection-associated high-mobility group box-3 ( Materials and Methods: A cross-sectional retrospective study was conducted amongst 50 Malay patients with NSCL/P who underwent surgery at Hospital Universiti Sains Malaysia (January 2022-January 2023). Participants were selected based on inclusion criteria from electronic medical records. Data on environmental and familial risk factors were obtained using validated pro formas, and Results: Cleft lip and palate (CL/P) were the most common deformity, accounting for 74% of cases, and 56% of patients were male. Significant risk factors for NSCL/P included consanguineous marriage, family history of clefts, maternal radiation exposure, traditional medicine use, allergies, paternal smoking and infant heart anomalies ( Discussion: The findings highlight complex gene-environment interactions in NSCL/P aetiology. Genetic predisposition, parental exposures and maternal factors jointly increase risk. Larger studies are needed to confirm these findings and further investigate gene-environment interactions in NSCL/P. The study underscores the role of

Indexed as

Cleft lip and palateenvironmental risk factorsgenetic predispositionnon-syndromic cleft lip and palatethymocyte selection-associated high-mobility group box-3 gene mutation

Identifiers

PMID42578177
PMCPMC13456629

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