Complex Genetic Architecture in RASopathies: Constitutional PTPN11 and Mosaic RIT1 Pathogenic Variants Underlying

Francesco Prevedello1, Dario Seif Ali1,2, Chiara Piccolo1,3

  • 1Department of Women's and Children's Health, University of Padova, Padova, Italy.

Summary

This study reports a rare case of Noonan syndrome (NS) in a patient with two distinct gene variants affecting the RAS/MAPK pathway, alongside acute myeloid leukemia (AML). The findings highlight the importance of comprehensive genetic testing for complex NS cases.

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