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The global epidemiology of acquired factor X deficiency

open access: yesHematology
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   +4 more sources

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

open access: yesThe 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   +3 more sources

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

open access: yesJournal 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   +3 more sources

Neonatal presentation of factor X deficiency

open access: yesIndian Journal of Health Sciences and Biomedical Research KLEU
Factor X is a Vitamin K-dependent serine protease synthesized in the liver. It is a key factor of the coagulation cascade as it is the first enzyme of a common pathway that leads to the formation of a stable fibrin clot.
Arjani Patra   +3 more
doaj   +2 more sources

Combined Factor VII and X Deficiency

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

Anticoagulation in atrial fibrillation with factor X deficiency—A management dilemma [PDF]

open access: yesClinical Case Reports, 2018
Key Clinical Message Factor X (FX) deficiency is a rare bleeding disorder. There is currently no clear guideline or recommendation for the appropriate selection of anticoagulation and management of patients with FX deficiency who require anticoagulation.
Jian Liang Tan   +3 more
doaj   +2 more sources

Plain language summary: What have research studies shown about plasma-derived human factor X concentrate treatment for people living with hereditary factor X deficiency? [PDF]

open access: yesTherapeutic Advances in Hematology
Summary What are these studies about? Researchers looked at the latest research studies about plasma-derived human factor X concentrate (pdFX for short) for people living with hereditary factor X deficiency (HFXD for short).
Miguel A. Escobar, Kaan Kavakli
doaj   +2 more sources

Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency

open access: yesHaematologica, 2008
Factor X deficiency is a severe rare hemorrhagic condition inherited as an autosomal recessive trait. It is one of the most severe recessive inherited coagulation disorders. We analyzed the clinical manifestations, laboratory phenotype and genotype in 10
Mehran Karimi   +4 more
doaj   +2 more sources

FACTOR-X DEFICIENCY: A RARE DISORDER TO BE LOOKED FOR IN CASES OF CONGENITAL BLEEDING TENDENCY [PDF]

open access: yesKhyber Medical University Journal, 2018
Factor X deficiency is a rare, autosomal recessive disorder that involves the coagulation cascade. People with this disorder present with a myriad of early life bleeding complications.
Fatima Ayaz   +2 more
doaj   +2 more sources

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