Myelodysplastic syndrome with multilineage dysplasia evolving to acute myeloid leukemia: Noonan syndrome with c.218C>T mutation in PTPN11 gene

Author:

Shenoy Rathika Damodara1ORCID,Yeshvanth Sunil Kumar2,Prasada L Harsha3,Shenoy Vijaya1,Shetty Vikram4

Affiliation:

1. Department of Paediatrics; K.S. Hegde Medical Academy; NITTE (Deemed to be University); Karnataka India

2. Department of Pathology; K.S. Hegde Medical Academy; NITTE (Deemed to be University); Karnataka India

3. Department of Pediatrics; Kasturba Medical College, Manipal Academy of Higher Education (Deemed to be University); Karnataka India

4. NITTE Meenakshi Institute of Craniofacial Surgery; NITTE (Deemed to be University); Karnataka India

Funder

Department of Health Research

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference13 articles.

1. OMIM. Noonan syndrome 1. Online Mendelian Inheritance in Man 2018 https://www.omim.org/entry/163950

2. Juvenile myelomonocytic leukaemia and Noonan syndrome;Strullu;J Med Genet,2014

3. How a rare pediatric neoplasia can give important insights into biological concepts: a perspective on juvenile myelomonocytic leukemia;Flotho;Haematologica,2007

4. Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation;Jongmans;Eur J Hum Genet,2011

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