Results 21 to 30 of about 567,487 (125)
Thrombosis and Haemostasis, 2021 Coagulation factor X (F10) amplifies the clotting reaction in the middle of the coagulation cascade, and thus F10 deficiency leads to a bleeding tendency.
A. Ichinose, T. Osaki, M. Souri
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Management of a patient with factor X deficiency with FEIBA: a case report
The 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
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Factor X deficiency: a comment on two recent case studies
The Journal of Haemophilia Practice, 2023 Hereditary factor X deficiency (HFXD) is a rare genetic bleeding disorder, affecting approximately 1 in 1,000,000 individuals globally, and resulting in abnormally low activity of clotting factor X (FX). Diagnosis may occur early in life, particularly in
Branchford Brian
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A case report of congenital factor X deficiency in an adult patient
SAGE 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
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Impact of Rare Bleeding Disorders during Pregnancy on Maternal and Fetal Outcomes: Review of 29 Pregnancies at a Single Center [PDF]
Revista Brasileira de Ginecologia e Obstetrícia, 2017 Objective: This study aims to give information about the relationship between different types of factor deficiencies and maternal/obstetric outcomes. Methods We retrospectively reviewed the medical records of eight women with factor deficiency disorders.
Gokcen Orgul +2 more
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Internal medicine, 2020 Acquired factor X deficiency (AFXD) is a very rare coagulation disorder. A 40-year-old man with no comorbidities suffering from a fever, malaise, and severe hemorrhagic symptoms, including massive hematuria, was emergently admitted.
S. Ichikawa +9 more
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Factor X Deficiency Management for Elective Cesarean Delivery in a Pregnant Patient
The American journal of case reports, 2020 Patient: Female, 39-year-old Final Diagnosis: Factor X deficiency Symptoms: Menstrual bleeding Medication: Solvent-detergent-treated fresh frozen plasma Clinical Procedure: Elective cesarean section Specialty: Obstetrics and Gynecology Objective: Rare co-
Mirna Krkovic +7 more
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The first reported case of factor X deficiency in a Filipino child – case study
The Journal of Haemophilia Practice, 2023 Factor X (FX) deficiency is an extremely rare inherited bleeding disorder affecting one in 1,000,000 people. According to the most recent published census of the World Hemophilia Federation, to date there is no reported case of FX deficiency in the ...
Masacupan Kristian Dorell +3 more
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Staged Surgical Palliation for HLHS in a Girl with Severe Factor X Deficiency
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
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Hemophilia A and factor V deficiency in a girl with Turner syndrome: a case report
Journal of Medical Case Reports, 2023 Background Hemophilia is an X-linked, recessive inherited disease caused by a defect or deficiency of one of the coagulation factors (VIII or IX). It is considered a rare disease in females.
Rawan Al khudari +3 more
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