Fanconi Anemia: Examining Guidelines for Testing All Patients with Hand Anomalies Using a Machine Learning Approach

• Päätekijät: Christoph Wallner (Tekijä), Jane Hurst (Tekijä), Björn Behr (Tekijä), Mohammad Abu Tareq Rony (Tekijä), Anthony Barabás (Tekijä), Gill Smith (Tekijä)
• Aineistotyyppi: Kirja
• Julkaistu: MDPI AG, 2022-01-01T00:00:00Z.
• Aiheet: article
• Linkit: Connect to this object online.

Background: This study investigated the questionable necessity of genetic testing for Fanconi anemia in children with hand anomalies. The current UK guidelines suggest that every child with radial ray dysplasia or a thumb anomaly should undergo further cost intensive investigation for Fanconi anemia...