Hiding in plain sight: Diagnosing congenital dysfibrinogenemia in a child presenting with acute myeloid leukemia-Reference-Cited by-同舟云学术

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Hiding in plain sight: Diagnosing congenital dysfibrinogenemia in a child presenting with acute myeloid leukemia

Published:2021-04-06 Issue:7 Volume:68 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Kumar Kriti¹,Patel Serina¹²,Chiang K. Y.³,Solh Ziad⁴⁵,Saleh Maha¹⁶,Ernewein Lauren⁷,Decourcy MaryJo⁷,Laudenbach Lori⁷,Tole Soumitra¹²^ORCID

Affiliation:

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

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.29050

Reference14 articles.

1. Early deaths and anti-hemorrhagic treatments in acute promyelocytic leukemia. A GIMEMA retrospective study in 268 consecutive patients [see comments]

2. Hypofibrinogenemia as a clue in the presumptive diagnosis of acute promyelocytic leukemia

3. Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management

4. Congenital Fibrinogen Disorders: An Update

5. Identification and characterization of novel mutations implicated in congenital fibrinogen disorders

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