Results 11 to 20 of about 1,017,222 (288)

Severe Congenital Factor X Deficiency as a First Case Report in Cambodia [PDF]

Case Reports in Hematology
Conclusion: FX deficiency, though rare, should be considered in the differential diagnosis of pediatric patients presenting with recurrent gingival or mucocutaneous bleeding in conjunction with prolonged PT and APTT.
Chin Soey, Meang Sovandos, Lam Pechkethia, Lean Kimsreng, Chean Sophâl   +4 more
doaj   +2 more sources

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

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

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

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

Factor X Deficiency [PDF]

American Society for Clinical Laboratory Science, 2010
1. Dorothy M (Adcock) Funk, M.D.[⇑][1] 1. Esoterix Coagulation, 8490 Upland Drive, Ste.100, Englewood, CO 80112 2. Dennis Casciato, M.D. 1. David Geffen School of Medicine at UCLA, Los Angeles, CA 90095-1732 1. Address for Correspondence: Dorothy M (Adcock) Funk, M.D., Esoterix Coagulation, 8490 Upland Drive, Ste.100, Englewood, CO ...
Dorothy M, Funk, Dennis, Casciato
openaire   +2 more sources

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
doaj   +1 more source

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