Pancytopenia, splenomegaly, and mild bony abnormalities secondary to novel variants in thromboxane synthetase: An unusual cause of bone marrow failure-Reference-Cited by-同舟云学术

Pancytopenia, splenomegaly, and mild bony abnormalities secondary to novel variants in thromboxane synthetase: An unusual cause of bone marrow failure

Published:2023-02-14 Issue:6 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Kowalczyk Alexandra¹,Chopra Yogi Raj²,Saleh Maha¹³,Colaiacovo Samantha³,Dror Yigal²^ORCID,Leppington Sarah⁴,Tole Soumitra¹⁵^ORCID

Affiliation:

1. Department of Pediatrics, Schulich School of Medicine & Dentistry Western University London Ontario Canada

2. Department of Pediatrics Division of Hematology/Oncology Hospital for Sick Children Toronto Ontario Canada

3. Medical Genetics Program of Southwestern Ontario London Health Sciences Centre London Ontario Canada

4. Children's Hospital London Health Sciences Centre London Ontario Canada

5. Department of Pediatrics, Division of Hematology/Oncology London Health Sciences Centre London Ontario Canada

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30253

Reference9 articles.

1. Ghosal hematodiaphyseal dysplasia: A rare cause of a myelophthisic anemia

2. Ghosal hematodiaphyseal dysplasia: a case report;Shakiba M;Int J Hematol Oncol Stem Cell Res,2020

3. Steroid-responsive Anemia in Patients of Ghosal Hematodiaphyseal Dysplasia

4. Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)

5. The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology