Results 161 to 170 of about 2,449 (204)
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Homeopathic Management of Afibrinogenemia along with Beta-Thalassemia
AYUHOM, 2022Afibrinogenemia is an extremely rare inherited bleeding disorder. Less than 100 such cases have been described from India. Beta-thalassemia carrier status (trait) is common in many Indian casts and religious groups; hence, a rare combination of these two
Kumat Omkar +4 more
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Pathogenic Mechanisms in Congenital Afibrinogenemia: A Systematic Review of Genetic Variants
HaemophiliaCongenital afibrinogenemia is a rare bleeding disorder characterized by the complete absence of plasma fibrinogen, primarily caused by homozygous or compound heterozygous mutations in the FGA, FGB and FGG genes.
Yang Li, Zirui Meng, Wei Qing, Ping Yi
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437 A case study of venous thromboembolism in a patient with congenital afibrinogenemia
American Journal of Clinical PathologyArterial and venous thromboembolism are known complications of congenital afibrinogenemia; however, management is challenging due to the lack of established guidelines for anticoagulation regimens.
Madison Guevara +5 more
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Afibrinogenemia with two compound heterozygous mutations in FGA gene
Haemophilia, 2021Fibrinogen is a 340 kDa hexameric glycoprotein synthetized by hepatocytes. It is composed by three polypeptide chains Aα, Bβ, and γ.1 Three genes are implicated in fibrinogen synthesis: FGA, FGB, and FGG for Aα, Bβ and γ chain respectively.2 Fibrinogen ...
G. Feugray +7 more
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Identification of a novel mutation in congenital afibrinogenemia in Iranian patients
Blood Coagulation and Fibrinolysis, 2021Congenital afibrinogenemia is a rare autosomal recessive disorder that is caused by defects in the fibrinogen. Fibrinogen is a hexameric glycoprotein made of two pairs of three homologous polypeptide chains including Aα, Bβ, and γ that are encoded by ...
S. Nojehdeh +4 more
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An unusual cause of intramedullary bone cysts – Congenital afibrinogenemia
Indian Journal of Musculoskeletal RadiologySolitary bone cysts have a wide range of differentials, but when there are numerous bone cysts involving multiple bone sites, a systemic hematological disorder would be the leading differential.
Raghu teja.S +3 more
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Thrombosis and Haemostasis, 1971
SummaryA case of congenital afibrinogenemia is reported.The patient is a 2 month old white female infant who presented bleeding from the umbilical stump a few days after birth. Subsequently other hemorrhagic manifestations were hematomas at the site of venipunctures.All routine plasmatic tests gave values greater than 1000 sec. The prothrombin time was
A Girolami, G Zacchello, R D’Elia
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SummaryA case of congenital afibrinogenemia is reported.The patient is a 2 month old white female infant who presented bleeding from the umbilical stump a few days after birth. Subsequently other hemorrhagic manifestations were hematomas at the site of venipunctures.All routine plasmatic tests gave values greater than 1000 sec. The prothrombin time was
A Girolami, G Zacchello, R D’Elia
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Congenital afibrinogenemia and splenic rupture: A case report
World Journal of Biology Pharmacy and Health SciencesCongenital afibrinogenemia is an extremely rare coagulation disorder affecting 1-2 individuals per million. We report the case of a 15-year-old male with known congenital afibrinogenemia who developed hemorrhagic shock following minor soccer ball trauma ...
Houda Guennouni Assimi +2 more
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Journal of Cardiothoracic and Vascular Anesthesia, 2020
Congenital afibrinogenemia is a rare autosomal recessive hematologic disorder that results in coagulopathy due to the complete lack of fibrinogen production.
Christine Choi, Timothy M. Maus
semanticscholar +1 more source
Congenital afibrinogenemia is a rare autosomal recessive hematologic disorder that results in coagulopathy due to the complete lack of fibrinogen production.
Christine Choi, Timothy M. Maus
semanticscholar +1 more source
Congenital Afibrinogenemia in Goats
Zentralblatt für Veterinärmedizin Reihe A, 2010Summary A case of congenital afibrinogenemia in goats is described. The animal shows severe haemorrhagic diathesis with joint bleedings. The patient's blood was absolutely incoagulable. Immunologically no fibrinogen could be demonstrated in the plasma. The other clotting factors were present in normal concentrations.
H J, Breukink +4 more
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