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Updated: Mar 24, 2026

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
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.
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.
Area of Science:
- Genetics
- Molecular Biology
- Oncology
Background:
- Noonan syndrome (NS) is a genetic disorder caused by RAS/MAPK pathway dysregulation.
- Complex genotypes, including multiple gene variants, are increasingly identified in NS.
- Concurrent NS and acute myeloid leukemia (AML) is rare.
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