Pancytopenia, splenomegaly, and mild bony abnormalities secondary to novel variants in thromboxane synthetase: An unusual cause of bone marrow failure
Pediatr Blood Cancer
.
2023 Jun;70(6):e30253.
doi: 10.1002/pbc.30253.
Epub 2023 Feb 14.
Authors
Alexandra Kowalczyk
1
,
Yogi Raj Chopra
2
,
Maha Saleh
1
3
,
Samantha Colaiacovo
3
,
Yigal Dror
2
,
Sarah Leppington
4
,
Soumitra Tole
1
5
Affiliations
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.
PMID:
36786374
DOI:
10.1002/pbc.30253
No abstract available
Publication types
Letter
MeSH terms
Bone Marrow
Bone Marrow Failure Disorders
Humans
Pancytopenia* / etiology
Splenomegaly
Thromboxane-A Synthase
Substances
Thromboxane-A Synthase