Results 21 to 30 of about 920,308 (229)

Staged Surgical Palliation for HLHS in a Girl with Severe Factor X Deficiency

The Thoracic & Cardiovascular Surgeon Reports, 2018
Background Factor X deficiency (also known as Stuart–Prower factor deficiency) is an autosomal recessive extremely rare hereditary hematologic disorder, affecting around 1:1,000,000 of the general population.
Ahmed F. Elmahrouk, Mohamed F. Ismail, Abdulbadee Bugis, Nashwa Badawy, Hesham Mohamed Aboelghar, Tamer Hamouda, Ahmed Jamjoom   +6 more
doaj   +2 more sources

Factor XDebrecen: Gly204Arg mutation in factor X causes the synthesis of a non-secretable protein and severe factor X deficiency

Haematologica, 2008
Due to a homozygous Gly204Arg mutation in the factor X (FX) gene no detectable FX antigen was found in the plasma of a one-year old patient with severe bleeding diathesis.
Zsuzsanna Bereczky, Helga Bárdos, István Komáromi, Csongor Kiss, Gizella Haramura, Éva Ajzner, Róza Ádány, László Muszbek   +7 more
doaj   +3 more sources

A viable mouse model of factor X deficiency provides evidence for maternal transfer of factor X [PDF]

, 2008
BackgroundActivated factor X (FXa) is a vitamin K-dependent serine protease that plays a pivotal role in blood coagulation by converting prothrombin to thrombin. There are no reports of humans with complete deficiency of FX, and knockout of murine F10 is
Shing Jen Tai, Roland W. Herzog, Paris Margaritis, Valder R. Arruda, K. Chu, J.A. GOLDEN, Patricia A. Labosky, Katherine A. High   +7 more
core   +7 more sources

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   +2 more sources

PB2326: SAFE AND EFFECTIVE PROPHYLAXIS WITH PLASMA-DERIVED FACTOR X CONCENTRATE IN AN ELDERLY PATIENT WITH HEREDITARY FACTOR X DEFICIENCY [PDF]

HemaSphere, 2022
H. Patel, S. Peltier, K. Clark, M. T. Reding   +3 more
doaj   +2 more sources

Cardiac Amyloidosis Presenting with Pre-Excitation Syndrome, Heart Failure, and Severe Factor X Deficiency as Part of Systemic Amyloid Light-Chain (AL) Amyloidosis - A Fatal Combination. [PDF]

Am J Case Rep, 2021
Almasri H, Almeer A, Awouda S, Hamid O, Sardar S, Anwer Z, Ibrahim F, Soliman D, Kandathil Y, Abu-Tineh M, Alabdul Razzak I, Alazawi SH.   +11 more
europepmc   +3 more sources

Pediatric split liver transplantation for congenital factor X deficiency: first 10-year follow-up of a case with portal vein stenting. [PDF]

Korean J Transplant, 2021
Namgoong JM, Hwang S, Kim DY, Ha TY, Song GW, Jung DH, Kim KM, Oh SH.   +7 more
europepmc   +3 more sources

Factor X deficiency presenting as an intracranial bleed in a young infant

Pediatric Hematology Oncology Journal
Inherited Factor X deficiency is a rare bleeding disorder. It is inherited in autosomal recessive manner. The genotype and the phenotype are variable. The management is tailored as per individual patient.
Sanyukta Sandeep Ghodke, Rishab Bhurat, Dhaarani Jayaraman, Sri Gayathri Shanmugam, Febe Renjitha Suman, Ramya Uppuluri, Rajakumar Padur Sivaraman, Julius Xavier Scott   +7 more
doaj   +2 more sources

Acquired-transient factor X deficiency in a teenager with extensive burns [PDF]

, 2011
Acquired factor X deficiency is an extremely rare situation. It has shown to be associated with systemic amyloidosis, respiratory mycoplasma infection, factor X inhibitors, antiphospholipid antibodies, vitamin K defi ciency/liver disease as well as the ...
André Mascarenhas, Mónica Eusébio, Orquídea Freitas, T. Almeida   +3 more
openalex   +3 more sources

Hemorrhage because of amyloid-related factor X deficiency after insertion of Tenckhoff catheter. [PDF]

Perit Dial Int, 2012
Harman G, McCormick BB.
europepmc   +3 more sources