Two cases of hepatoblastoma in Bohring–Opitz syndrome: An emerging association-Reference-Cited by-同舟云学术

Two cases of hepatoblastoma in Bohring–Opitz syndrome: An emerging association

Published:2024-04-18 Issue:7 Volume:71 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Patel Kritika¹²^ORCID,McQuaid Shelly³⁴,Ketterl Tyler¹²^ORCID,Benedetti Daniel J.⁵^ORCID,Sokol Elizabeth³⁴^ORCID

Affiliation:

1. Cancer and Blood Disorders Center Seattle Children's Hospital Seattle Washington USA

2. Division of Hematology/Oncology and Bone Marrow Transplant Department of Pediatrics University of Washington Seattle Washington USA

3. Ann & Robert H. Lurie Children's Hospital of Chicago Chicago Illinois USA

4. Division of Hematology Oncology, Neuro‐Oncology and Stem Cell Transplantation Department of Pediatrics Northwestern University Feinberg School of Medicine Chicago Illinois USA

5. Division of Hematology/Oncology Department of Pediatrics Vanderbilt University Medical Center Nashville Tennessee USA

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.31010

Reference6 articles.

1. Clinical management of patients withASXL1mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance

2. Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma

3. A case of probable Bohring–Opitz syndrome with medulloblastoma

4. Clinical findings in 39 individuals with Bohring–Opitz syndrome from a global patient‐driven registry with implications for tumor surveillance and recurrence risk

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