Results 71 to 80 of about 975,682 (206)

DUA KASUS ACQUIRED PROTHROMBIN COMPLEX DEFICIENCY DENGAN PERDARAHAN INTRAKRANIAL : LAPORAN KASUS

JKS (Jurnal Kedokteran Syiah Kuala), 2017
Abstrak. Acquired Prothrombin Complex Deficiency (APCD) merupakan perdarahan spontan yang disebabkan oleh penurunan aktivitas faktor koagulasi yang tergantung vitamin K (faktor II, VII, IX dan X), sedangkan aktivitas faktor koagulasi lain, kadar ...
Jufitriani Ismy
doaj   +1 more source

Circulating Inhibitor against Factor X: A Rare Cause of Hemorrhagic Diathesis

Case Reports in Hematology, 2023
Acquired coagulopathies resulting from factor X deficiency are rare and typically associated with amyloidosis or plasma cell dyscrasia. Factor X plays a pivotal role in the coagulation cascade, converting prothrombin into thrombin and facilitating the ...
P. Rossignon, F. Grandjean, A. Claessens, N. Weynants   +3 more
doaj   +1 more source

Review Dental Treatment of Patients with Congenital Bleeding Disorders

Česká Stomatologie a Praktické Zubní Lékařství, 2014
Objectives: The commonest congenital bleeding disorders in childhood are hemophilia, von Willebrand disease and deficiency of factor XI. Disease is characterized by a deficient of coagulability. It is a gonosomal recessive condition.
J. Papež, K. Chleborád, T. Dostálová
doaj   +1 more source

Factor X Concentrate Treatment Schedule and Dosing in Acquired FX Deficiency

Hematology Reports
Background: Acquired factor X (FX) deficiency is a rare condition that can cause life threatening bleeding. Here we outline a successful management strategy for gastrointestinal bleeding (GI) using human FX concentrate.
Andrew Ross, Rebecca J. Shaw, Louise Garth, Cathy Farrelly   +3 more
doaj   +1 more source

A Case of Haemorrhages caused by Multiple Myeloma Induced Factor Deficiencies: A Bleeding Enigma [PDF]

Journal of Clinical and Diagnostic Research
A 74-year-old male patient presented with anaemia, thrombocytopenia, and extensive haemorrhages over both thighs and back. A coagulation work-up revealed markedly elevated Prothrombin Time (PT) and activated Partial Thromboplastin Time (aPTT).
Abhijith Lakshman, Febe Renjitha Suman, Gramani Arumugam Vasugi, Uma Lakshmi Ramdoss   +3 more
doaj   +1 more source

FACTOR-X DEFICIENCY: A RARE DISORDER TO BE LOOKED FOR IN CASES OF CONGENITAL BLEEDING TENDENCY [PDF]

Khyber Medical University Journal, 2018
Factor X deficiency is a rare, autosomal recessive disorder that involves the coagulation cascade. People with this disorder present with a myriad of early life bleeding complications.
Fatima Ayaz, Saeed Bin Ayaz, Muhammad Furrukh   +2 more
doaj  

Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function

Haematologica, 2010
Background Severe hereditary coagulation factor XIII deficiency is a rare homozygous bleeding disorder affecting one person in every two million individuals. In contrast, heterozygous factor XIII deficiency is more common, but usually not associated with
Vytautas Ivaskevicius, Arijit Biswas, Carville Bevans, Verena Schroeder, Hans Peter Kohler, Hannelore Rott, Susan Halimeh, Petro E. Petrides, Harald Lenk, Manuele Krause, Bruno Miterski, Ursula Harbrecht, Johannes Oldenburg   +12 more
doaj   +1 more source

Partial gene deletion in a family with factor X deficiency [PDF]

, 1989
Fabı́ola Del Carlo Bernardi, Giovanna Marchetti, P. Patracchini, Stefano Volinia, Donato Gemmati, Paolo Simioni, A Girolami   +6 more
openalex   +3 more sources

Acquired factor X deficiency in systemic amyloidosis

Cleveland Clinic Journal of Medicine, 1987
Acquired factor X deficiency has been described in association with primary amyloidosis in a small number of patients. Although readily corrected in vitro by mixing patient plasma with normal plasma, the deficiency is not easily corrected in vivo because transfused factor X is rapidly cleared from the circulation.
F V, Lucas, A J, Fishleder, R C, Becker, D S, Cavalier, R R, Tubbs   +4 more
openaire   +2 more sources

Diagnosis, therapeutic advances, and key recommendations for the management of factor X deficiency.

Blood reviews, 2021
F. Peyvandi, G. Auerswald, S. Austin, R. Liesner, K. Kavaklı, M. Á. Álvarez Román, C. Millar   +6 more
semanticscholar   +1 more source