Hiding in plain sight: Diagnosing congenital dysfibrinogenemia in a child presenting with acute myeloid leukemia
Pediatr Blood Cancer
.
2021 Jul;68(7):e29050.
doi: 10.1002/pbc.29050.
Epub 2021 Apr 6.
Authors
Kriti Kumar
1
,
Serina Patel
1
2
,
K Y Chiang
3
,
Ziad Solh
4
5
,
Maha Saleh
1
6
,
Lauren Ernewein
7
,
MaryJo Decourcy
7
,
Lori Laudenbach
7
,
Soumitra Tole
1
2
Affiliations
1
Department of Pediatrics, Schulich School of Medicine & Dentistry, Western University, London, Ontario, Canada.
2
Division of Hematology/Oncology, Department of Pediatrics, London Health Sciences Centre, London, Ontario, Canada.
3
Division of Hematology/Oncology, Department of Pediatrics, Hospital for Sick Children, Toronto, Ontario, Canada.
4
Department of Pathology and Laboratory Medicine (PaLM), Western University, London, Ontario, Canada.
5
Department of Medicine, Schulich School of Medicine & Dentistry, Western University, London, Ontario, Canada.
6
Medical Genetics Program of Southwestern Ontario, London Health Sciences Centre, London, Ontario, Canada.
7
Children's Hospital, London HealthSciences Centre, London, Ontario, Canada.
PMID:
33822462
DOI:
10.1002/pbc.29050
No abstract available
Publication types
Letter
MeSH terms
Afibrinogenemia* / complications
Afibrinogenemia* / diagnosis
Child
Family
Humans
Leukemia, Myeloid, Acute* / complications
Leukemia, Myeloid, Acute* / diagnosis
Supplementary concepts
Dysfibrinogenemia, Congenital