Factor X deficiency: An overlooked cause of bleeding in the newborn [PDF]
Asian Journal of Transfusion ScienceInherited 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
Acquired factor X deficiency in a patient with multiple myeloma: a rare case highlighting the significance of comprehensive evaluation and the need for antimyeloma therapy for bleeding diathesis. [PDF]
BMJ Case Rep, 2019 Factor X deficiency is a rare bleeding disorder that can be associated with life-threatening bleeding events. Factor X deficiency can either be inherited or acquired.
Reynolds SB, Maghavani DP, Hashmi H.
europepmc +2 more sources
The global epidemiology of acquired factor X deficiency [PDF]
HematologyObjectives 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
Combined Factor VII and X Deficiency [PDF]
Online 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
Staged Surgical Palliation for HLHS in a Girl with Severe Factor X Deficiency [PDF]
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 +6 more
doaj +2 more sources
The Long-term Outcomes after VAD plus SCT Therapy in a Patient with AL Amyloidosis and Severe Factor X Deficiency. [PDF]
Intern 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 +2 more sources
Definitions, 2004 Factor X deficiency is a rare bleeding disorder that varies in severity among affected individuals. The signs and symptoms of this condition can begin at any age, although the most severe cases are apparent in childhood.
F. Vianello
semanticscholar +3 more sources
Use of prothrombin complex concentrate for prophylaxis of bleeding in acquired factor X deficiency associated with light-chain amyloidosis. [PDF]
Blood Transfus, 2016 Veneri D +6 more
europepmc +3 more sources
Haemophilia, 2016 Hereditary factor X (FX) deficiency affects 1:500 000 to 1:1 000 000 of individuals. There are few published data on the pharmacokinetics (PK) of FX for existing treatments for FX deficiency, and no specific replacement factor concentrate exists.
Steve Austin +5 more
openalex +2 more sources
Efficacy, safety and pharmacokinetics of a new high‐purity factor X concentrate in subjects with hereditary factor X deficiency [PDF]
Haemophilia, 2016 Hereditary factor X (FX) deficiency is a rare bleeding disorder affecting 1:500 000 to 1:1 000 000 of individuals. Until recently, no specific replacement factor concentrate was available.
Steve Austin +5 more
openalex +2 more sources