نتایج جستجو برای: factor v deficiency

تعداد نتایج: 1240345  

Journal: :Blood 2003
Ophira Salomon Ariella Zivelin Tami Livnat Rima Dardik Ron Loewenthal Ophelia Avishai David M Steinberg Michael H Rosove Niamh O'Connell Christine A Lee Uri Seligsohn

Factor XI deficiency, an injury-related bleeding disorder, is rare worldwide but common in Jews in whom 2 mutations, Glu117Stop (type II) and Phe283Leu (type III), prevail. Mean factor XI activities in homozygotes for Glu117Stop and for Phe283Leu are 1 and 10 U/dL, respectively. Inhibitors to factor XI in patients with severe factor XI deficiency have been reported in a small number of instance...

Journal: :Journal of Neurology, Neurosurgery & Psychiatry 1992

Journal: :Seminars in Thrombosis and Hemostasis 2019

Journal: :Blood 1989
F Bernardi G Marchetti P Patracchini S Volinia D Gemmati P Simioni A Girolami

The presence of gene lesions in coagulation factor X (FX, Stuart factor) was investigated in patients with FX deficiency or an FX abnormality (FX Friuli). The proposita had a heterozygous partial deletion of the FX gene with severe deficiency of FX activity and antigen. The lesion, which was inherited from her mother, removes the 3' portion of the gene coding for the catalytic domain of the fac...

Journal: :Papua and New Guinea medical journal 1997
M Sapuri A B Amoa G Kariwiga J White

Factor V deficiency is a rare hereditary disorder. We report a patient with factor V deficiency who presented with menorrhagia and pelvic haematoma. The Haematology Department at the Royal Brisbane Hospital performed the definitive factor assays leading to the diagnosis. The challenges of her management were obtaining adequate supplies of factor V and her socioeconomic circumstances. The main f...

Journal: :Thrombosis and haemostasis 2008
Daniel Delev Anna Pavlova Stefan Heinz Mathias Costa Blaise Tamir Chandra Bernd Poetsch Erhard Seifried Johannes Oldenburg

Human coagulation factor V (FV), a non-enzymatic cofactor of the prothrombinase complex, is required for the rapid generation of thrombin. FV deficiency is a rare autosomal recessive bleeding disorder. We describe two novel mutations, Tyr91Asn and Asp2098Tyr, found in two probands with a residual FV activity of 51% and 4%, respectively. Modelling and structural analysis of these mutations were ...

2017
Arshi Naz Muhammad Younus Jamal Samina Amanat Ikram Din Ujjan Akber Najmuddin Humayun Patel Fazle Raziq Nisar Ahmed Ayisha Imran Tahir Sultan Shamsi

BACKGROUND Autosomal recessive bleeding disorders (ARBDs) include deficiencies of clotting factors I, II, V, VII, X, XI, XIII, vitamin K dependent clotting factors, combined factor V & VIII, Von Willebrand Disease (vWD) type 3, Glanzmann's thrombasthenia (GT) and Bernard-Soulier syndrome. Patients with primary bleeding disorders from all the major provincial capitals of Pakistan were screened f...

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