ArticleOrphanet journal of rare diseases2025
Renal MRI radiomics in Beckwith-Wiedemann syndrome: a novel imaging approach for genotype identification.
Article in Orphanet journal of rare diseases, 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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Authors and funding
7 authors.
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Abstract
purposeTo valuate the role of nonmalignant nephrological findings and renal MRI radiomics in differentiating molecular subtypes of Beckwith-Wiedemann syndrome (BWS). MATERIALS AND
methodsClinical data and abdominal MRI scans of 49 patients who underwent partial glossectomy between July 2019 and March 2024 were retrospectively analysed. Patients were categorized into two subtypes: BWS
resultsClinically, the BWS
conclusionNonmalignant renal abnormalities and MRI radiomics models have potential as alternative imaging tools for the identification of renal predisposition genotypes and the surveillance of renal size change in BWS patients.
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