Evidence map›Paper›PMID 41230207›Full record

ArticleMolecular syndromology2025

Clinical and Molecular Evaluation of Beckwith-Wiedemann Syndrome with the BWSICS Score.

Duygu Çetinkaya, Mustafa Altan, Esra Kılıç

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Article in Molecular syndromology, 2025. 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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5 · Who and what money

Authors and funding

3 authors.

Duygu ÇetinkayaDepartmant of Pediatric Genetics, University of Health Sciences, Ankara Bilkent City Hospital, Ankara, Turkey.
Mustafa AltanDepartment of Medical Genetics, Ankara Bilkent City Hospital, Ankara, Turkey.
Esra KılıçDepartmant of Pediatric Genetics, University of Health Sciences, Ankara Bilkent City Hospital, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Beckwith-Wiedemann syndrome (BWS, MIM#130650) is an overgrowth syndrome characterized by macroglossia, omphalocele, macrosomia, and a predisposition to neoplasia. The etiology of BWS involves genetic and epigenetic alterations in the 11p15 region of the genome. In this study, we investigated how the International Consensus Clinical Scoring System (BWSICS) score can be used in clinical and molecular evaluations and examined its contribution to diagnostic processes. Methods: This retrospective study included BWS patients who have been followed up in the pediatric genetics clinic of a center in the last 10 years. Clinical and molecular outcomes including chromosome analysis, microarray analysis, and MS-MLPA testing were evaluated. BWSICS scores were calculated for each patient based on their clinical symptoms. Results: The study evaluated 18 patients who met BWS diagnostic criteria aged between 1 day and 10 years. The main presentations were macroglossia in 4 patients, omphalocele with macroglossia in 5 patients, and hypoglycemia in 2 patients and all but 1 patient was macrosomia. Significant congenital malformations included omphalocele and visceromegaly in 5 patients each. Hepatoblastoma was observed in 1 patient and 1 patient died due to sepsis. Two patients had autism spectrum disorder while the others had normal neuromotor development. According to the BWSICS, patients' scores ranged from 5 to 11. Molecular analysis revealed methylation alterations in 13/16 patients. Conclusion: This study examined the effectiveness of the BWSICS score in the diagnosis and follow-up of BWS in combination with clinical and molecular evaluation. This score provides a broad assessment in the diagnosis of BWS and can be considered as an important tool in clinical practice.

Indexed as

Beckwith-Wiedemann syndromeMacroglossiaMultiplex ligation-dependent probe amplificationOvergrowth syndrome

Identifiers

PMID41230207
PMCPMC12603577

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