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

open access: yesBrazilian 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   +2 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

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: yesJournal 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   +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

Combined Factor VII and X Deficiency [PDF]

open access: yesOnline Journal of Health & Allied Sciences, 2011
Factor VII deficiency and factor X deficiency and very rare disorders individually. Combined Factor VII and X is a rare congenital blood disorder with very few cases reported in the literature.
Gursharan Singh Narang,   +2 more
doaj   +1 more source

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   +2 more sources

A rare case of factor X deficiency induced by valproic acid [PDF]

open access: yesResearch and Practice in Thrombosis and Haemostasis
Background: Factor X (FX) deficiency (FXD) significantly disrupts coagulation, potentially leading to severe bleeding. While inherited FXD is rare, with a prevalence of 1 in 500,000, acquired FXD is also uncommon and frequently linked to conditions such ...
Pierre-Antonin Rigon, Vincent Ernest
doaj   +2 more sources

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

open access: yesAsian Journal of Transfusion Science
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   +2 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   +2 more sources

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