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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   +5 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   +3 more sources

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

Factor X deficiency: An overlooked cause of bleeding in the newborn [PDF]

open access: diamondAsian Journal of Transfusion Science, 2023
Inherited factor X (FX) deficiency is a rare autosomal recessive bleeding disorder, presenting with various bleeding manifestations ranging from nonspecific bruising to life-threatening intracranial hemorrhage.
Shalini Verma   +2 more
doaj   +3 more sources

Plasma‐derived factor X concentrate compassionate use for hereditary factor X deficiency: Long‐term safety and efficacy in a retrospective data‐collection study [PDF]

open access: yesResearch and Practice in Thrombosis and Haemostasis, 2021
Background Coagadex is a high‐purity plasma‐derived factor X concentrate (pdFX) developed to treat hereditary factor X deficiency (FXD). Objective Evaluate the efficacy and safety of pdFX administered to patients with hereditary FXD.
James N. Huang   +4 more
doaj   +3 more sources

Inherited Moderate Factor X Deficiency Presenting as Cardiac Tamponade [PDF]

open access: yesCase Reports in Hematology, 2019
Factor X deficiency is a rare bleeding disorder that varies in the severity of its clinical manifestations. The symptoms of this disorder can occur at any age, although most severe cases appear in childhood.
Tamer Othman   +4 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

The Long-term Outcomes after VAD plus SCT Therapy in a Patient with AL Amyloidosis and Severe Factor X Deficiency. [PDF]

open access: diamondIntern Med, 2018
A 55-year-old man was admitted to our institute to undergo evaluation for proteinuria (5.4 g/day) with lambda-type Bence-Jones protein (BJP). Primary amyloid light chain (AL) amyloidosis and acquired factor X deficiency were diagnosed.
Iwadate D   +16 more
europepmc   +4 more sources

Post-COVID Factor X Deficiency: A Case Report From Pakistan. [PDF]

open access: yesCureus, 2022
Acquired Factor X deficiency is a rare hematological disease, characterized by excessive bleeding, with fewer than 50 cases reported in the literature and practically all being associated with amyloidosis.
Humayun O   +4 more
europepmc   +2 more sources

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