Multiple synchronous malignancies in an infant with concomitant homozygous <i>BRCA2</i> and <i>PMS2</i> mutations with Fanconi anemia phenotype-Reference-Cited by-同舟云学术

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Multiple synchronous malignancies in an infant with concomitant homozygous BRCA2 and PMS2 mutations with Fanconi anemia phenotype

Published:2023-02-02 Issue:6 Volume:40 Page:587-594
ISSN:0888-0018
Container-title:Pediatric Hematology and Oncology
language:en
Short-container-title:Pediatric Hematology and Oncology

Author:

Alghanim Hamad Mohammed¹,Eltawel Mohamed¹²³,Alhaidari Abdulmajeed Ibrahim¹,Alobaid Muhannad Mohammed¹,Moghairi Areej Mofareh¹⁴³,Sufiani Fahad¹⁵³,Ahmad Naveed¹²³^ORCID

Affiliation:

1. Department of Pediatric Hematology Oncology, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia

2. Department of Pediatric Hematology & Oncology, King Abdullah Specialized Children’s Hospital, Riyadh, Saudi Arabia

3. King Abdullah International Medical Research Center, Riyadh, Saudi Arabia

4. Department of Pathology and Laboratory Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia

5. Department of Pathology & Laboratory Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/08880018.2022.2154417

Reference20 articles.

1. Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations

2. Germline truncating mutations in both MSH2 and BRCA2 in a single kindred

3. Double heterozygosity in the BRCA1 and BRCA2 genes in Italian family

4. Multiple primary tumours: challenges and approaches, a review

5. Predisposition to cancer in children and adolescents

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