Spectrum of afibrinogenemia: Bleeding to thrombosis- retrospective analysis of five patients

Background: Afibrinogenemia is a rare disorder, with autosomal recessive inheritance, most often associated with consanguinity. To date, very few cases have been reported from India. The aim was to study the clinical heterogenicity of patients with afibrinogenemia. Case series: We present a retrospe...

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Bibliographic Details

Published in:	Pediatric Hematology Oncology Journal
Main Authors:	Sneha Waghela, Sujata Sharma, Nikita Shah, Harshada Uchil, Radha Ghildiyal
Format:	Article
Language:	English
Published:	Elsevier 2024-03-01
Subjects:	Afibrinogenemia Bleeding Hemostasis Thrombosis Umbilical cord bleeding
Online Access:	http://www.sciencedirect.com/science/article/pii/S2468124523003546