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Anesthesia strategy for factor X deficiency coagulopathy: case report [PDF]

open access: diamondBrazilian Journal of Anesthesiology, 2022
Factor X deficiency ranks among the rarest coagulopathies and has a variable presentation spectrum. We intend to present a proposal for anesthesia protocol for individuals with the coagulopathy.
Carla Isabel Ferreira   +5 more
doaj   +3 more sources

Successful Treatment of Factor X Deficiency in a Patient with Lymphoplasmacytic Lymphoma with Bendamustine Plus Rituximab Regimen: A Case Report and Literature Review [PDF]

open access: goldJournal of Blood Medicine, 2021
Tarinee Rungjirajittranon, Yingyong Chinthammitr, Chattree Hantaweepant Division of Hematology, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, ThailandCorrespondence: Chattree HantaweepantClinical Lecturer of ...
Rungjirajittranon T   +2 more
doaj   +4 more sources

Acquired Factor X Deficiency in Patients With Primary Light Chain Amyloidosis [PDF]

open access: goldJournal of Investigative Medicine High Impact Case Reports, 2019
Acquired factor X (FX) deficiency is a rare but serious complication of primary amyloidosis, presumably caused by the binding of amyloid proteins to the clotting factors.
Siroj Dejhansathit MD   +1 more
doaj   +4 more sources

A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female [PDF]

open access: yesCase Reports in Hematology, 2021
Factor X deficiency is a rare coagulopathy that can be inherited or acquired. Acquired factor X deficiency has been associated with plasma cell dyscrasias, amyloids, and use of vitamin K antagonists.
Ayrton Bangolo   +6 more
doaj   +2 more sources

A case report of congenital factor X deficiency in an adult patient [PDF]

open access: yesSAGE Open Medical Case Reports, 2022
Factor X deficiency is one of the rarest coagulation disorders representing 10% of all rare bleeding diseases with a frequency of 1:1,000,000. A 39-year-old male patient with no previous medical conditions was admitted to the hospital with a left carpal ...
Rehab Y AL-Ansari   +3 more
doaj   +2 more sources

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

open access: bronze, 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   +3 more
openalex   +3 more sources

The global epidemiology of acquired factor X deficiency [PDF]

open access: goldHematology
Objectives To summarize available data and contribute to a broader understanding of the global incidence and prevalence of acquired factor X deficiency.Methods A comprehensive review of English-language publications from PubMed and Embase was conducted ...
Kristy Iglay   +4 more
doaj   +2 more sources

Management of a patient with factor X deficiency with FEIBA: a case report

open access: diamondThe Journal of Haemophilia Practice, 2023
Hereditary factor X (FX) deficiency is a rare autosomal recessive disorder that increases bleeding tendencies, ranging from epistaxis to intracranial haemorrhage (ICH), which can be life-threatening.
Borboruah Luish, Dutta Anupam
doaj   +2 more sources

Acquired Factor X Deficiency without Amyloidosis Presenting with Massive Hematuria: A Case Report and Review of the Literature [PDF]

open access: yesHematology Reports, 2023
Acquired factor X deficiency is a rare diagnosis, especially without the association of other co-existing conditions such as amyloidosis. The authors report the case of a 34-year-old male with severe frank hematuria found to have markedly prolonged ...
Sasmith R. Menakuru   +3 more
doaj   +2 more sources

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

open access: green, 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   +7 more
openalex   +4 more sources

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