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...
Saved in:
Main Authors: | Sneha Waghela (Author), Sujata Sharma (Author), Nikita Shah (Author), Harshada Uchil (Author), Radha Ghildiyal (Author) |
---|---|
Format: | Book |
Published: |
Elsevier,
2024-03-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Varied clinical presentation of compound heterozygous thalassemia with delta beta or hereditary persistence of foetal hemoglobin
by: Sneha Waghela, et al.
Published: (2023) -
Alloimmunization in children with sickle cell disease: A tertiary care experience
by: Sujata Sharma, et al.
Published: (2023) -
Congenital Afibrinogenemia presenting as antenatal intracranial bleed: a case report
by: Parapurath Rajiv, et al.
Published: (2010) -
A study of the adverse drug reactions of L-asparaginase in newly diagnosed children with acute lymphoblastic leukemia
by: Harshada Uchil, et al.
Published: (2017) -
Afibrinogenemia en el embarazo
by: Rafael Quiñones Daza
Published: (1955)