Occurrence of high‐grade glioma in Noonan syndrome: Report of two cases-Reference-Cited by-同舟云学术

Occurrence of high‐grade glioma in Noonan syndrome: Report of two cases

Published:2019-01-28 Issue:5 Volume:66 Page:e27625
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

El‐Ayadi Moatasem¹²³⁴^ORCID,Ansari Marc¹²,Kühnöl Caspar D.⁵,Bendel Anne⁶^ORCID,Sturm Dominik⁷⁸,Pietsch Torsten⁹,Kramm Christof M.¹⁰,Bueren André O.¹²^ORCID

Affiliation:

1. Division of Pediatric Hematology and OncologyDepartment of Pediatrics and Adolescent MedicineUniversity Hospital of Geneva Geneva Switzerland

2. Department of PediatricsCANSEARCH Research LaboratoryFaculty of MedicineUniversity of Geneva Geneva Switzerland

3. Department of Pediatric OncologyNational Cancer InstituteCairo University Giza Egypt

4. Department of Pediatric OncologyChildren's Cancer Hospital Cairo Egypt

5. Department of Pediatric Hematology/OncologyUniversity Hospital HalleClinic and Polyclinic for Pediatrics IFaculty of MedicineMartin‐Luther‐University Halle‐Wittenberg Halle Germany

6. Department of Pediatric Hematology/OncologyChildren's Minnesota Minneapolis Minnesota

7. Division of Pediatric NeurooncologyGerman Cancer Research Center (DKFZ)Hopp‐Children's Cancer Center at the NCT HeidelbergGerman Consortium for Translational Cancer Research (DKTK) Heidelberg Germany

8. Department of Pediatric OncologyHematologyImmunology and PulmonologyHeidelberg University Hospital Heidelberg Germany

9. Institute of NeuropathologyDGNN Brain Tumor Reference CenterUniversity of Bonn Medical Center Bonn Germany

10. Division of Pediatric Hematology and OncologyUniversity Medical Center Goettingen Göttingen Germany

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.27625

Reference15 articles.

1. Hypertelorism With Turner Phenotype

2. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

3. Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia

4. Malignancy in Noonan syndrome and related disorders

5. Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes

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