Laboratory and molecular diagnosis of factor XI deficiency

S Davidson, K Gomez - Seminars in Thrombosis and …, 2024 - thieme-connect.com
The prevalence of factor XI (FXI) deficiency is 1 per 10 to 20,000 in the general population,
much higher than that reported in most texts. The prevalence is higher in Ashkenazi Jews …

Factor XI deficiency: phenotypic age-related considerations and clinical approach towards bleeding risk assessment

AA Barg, T Livnat, G Kenet - Blood, 2024 - Elsevier
Factor XI (FXI) deficiency is a rare bleeding disorder that presents complex challenges in
patient assessment and bleeding risk management. Despite generally causing mild to …

[HTML][HTML] Rare bleeding disorders: Real-world data from a Spanish tertiary hospital

D Martínez-Carballeira, A Caro, Á Bernardo… - Blood Cells, Molecules …, 2024 - Elsevier
Introduction Due to their low prevalence, rare bleeding disorders (RBDs) remain poorly
characterized. Aim To gain insight of RBDs through our clinical practice. Methods …

Cerebral sinus venous thrombosis in children with inherited bleeding disorders: A case series

IN Sheikh, L Srivaths, E Li… - Pediatric Blood & …, 2022 - Wiley Online Library
In patients with inherited bleeding disorders, thrombus development poses a challenge in
balancing the management of thrombosis and bleeding. Pediatric antithrombotic therapy …

Brief Overview about Inherited Rare coagulation disorders

LM Sherief, M Zakaria, AA Abd El Fattah… - Zagazig University …, 2024 - journals.ekb.eg
Background: Numerous rare congenital bleeding disorders include fibrinogen and
prothrombin deficiency as well as factor (V, VII, VIII, XI, X, and XIII) deficiency. In the general …

Rare Inherited Coagulation Factor Deficiencies

JLVSB Muhammad, F Khananic… - SickKids Handbook of …, 2017 - books.google.com
Rare inherited coagulation disorders other than factor VIII (FVIII) and factor IX (FIX)
deficiencies and von Willebrand disease present clinical challenges in both diagnosis and …