Results 11 to 20 of about 436,501 (200)

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, Mohamed F. Ismail, Abdulbadee Bugis, Nashwa Badawy, Hesham Mohamed Aboelghar, Tamer Hamouda, Ahmed Jamjoom   +6 more
doaj   +2 more sources

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

Journal 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, Attaya Suvannasankha MD   +1 more
doaj   +2 more sources

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

Clinical 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, Kah Poh Loh, Danielle Fortuna, Arezoo Ghaneie   +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]

Therapeutic 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

PB2326: SAFE AND EFFECTIVE PROPHYLAXIS WITH PLASMA-DERIVED FACTOR X CONCENTRATE IN AN ELDERLY PATIENT WITH HEREDITARY FACTOR X DEFICIENCY [PDF]

HemaSphere, 2022
H. Patel, S. Peltier, K. Clark, M. T. Reding   +3 more
doaj   +2 more sources

PB2319: ACQUIRED COAGULOPATHY: FACTOR X DEFICIENCY AT DIAGNOSIS OF MULTIPLE MYELOMA WITHOUT ASSOCIATED AMYLOIDOSIS [PDF]

HemaSphere, 2022
M. De La Torre De La Paz, G. Figaredo García Mina, A. Guerrero Díez, A. Rodríguez Alén, M. D. L. O. Abío Calvete, N. Rollón Simón, J. Cuesta Tovar   +6 more
doaj   +2 more sources

Gastrointestinal Bleeding From Acquired Factor X Deficiency due to Light Chain Amyloidosis [PDF]

Gastro Hep Advances
Kyle S. Liu, Xiuli Liu, Elizabeth Blaney
doaj   +2 more sources

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, Fatih Aktoz, M. Sinan Beksac   +2 more
doaj   +1 more source

Factor XDebrecen: Gly204Arg mutation in factor X causes the synthesis of a non-secretable protein and severe factor X deficiency

Haematologica, 2008
Due to a homozygous Gly204Arg mutation in the factor X (FX) gene no detectable FX antigen was found in the plasma of a one-year old patient with severe bleeding diathesis.
Zsuzsanna Bereczky, Helga Bárdos, István Komáromi, Csongor Kiss, Gizella Haramura, Éva Ajzner, Róza Ádány, László Muszbek   +7 more
doaj   +1 more source

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, Duaa Batesh, Roaa Habash, Othman Hamdn   +3 more
doaj   +1 more source