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About Congenital Afibrinogenemia.
Turkish journal of haematology : official journal of Turkish Society of Haematology, 2016 openaire +1 more source
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American Journal of Hematology, 1994
AbstractCongenital afibrinogenemia is a rare disorder with unusual clinical manifestations. The disease is inherited as an autosomal recessive trait and consanguinity is common among affected families. Clinical manifestations range from minimal bleeding to catastrophic hemorrhage.
Hamid Al-Mondhiry +2 more
exaly +3 more sources
AbstractCongenital afibrinogenemia is a rare disorder with unusual clinical manifestations. The disease is inherited as an autosomal recessive trait and consanguinity is common among affected families. Clinical manifestations range from minimal bleeding to catastrophic hemorrhage.
Hamid Al-Mondhiry +2 more
exaly +3 more sources
A case of congenital afibrinogenemia
Research in Clinic and Laboratory, 1983A case of congenital afibrinogenemia is described. In the family studied, the defect is transmitted as an autosomal recessive trait. The possible heterogeneity of congenital afibrinogenemia is discussed.
A, Galletti +3 more
exaly +3 more sources
Pediatrics, 1954
A case of congenital afibrinogenemia is described. Despite the absolute incoagulability of afibrinogenemic blood, this type of hemorrhagic diathesis is not accompanied by hemarthrosis. Systematic studies of this patient's blood revealed that all other known clotting factors are present in normal concentration.
P G, FRICK, I, McQUARRIE
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A case of congenital afibrinogenemia is described. Despite the absolute incoagulability of afibrinogenemic blood, this type of hemorrhagic diathesis is not accompanied by hemarthrosis. Systematic studies of this patient's blood revealed that all other known clotting factors are present in normal concentration.
P G, FRICK, I, McQUARRIE
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Acta Paediatrica, 1963
SUMMARYTwo patients, brother and sister, suffering from congenital afibrinogenemia are reported. This condition has previously not been described from Scandinavia. Both suffered from severe umbilical hemorrhage soon after birth and a continuing bleeding tendency.
S, OSEID, H M, SVENDSEN
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SUMMARYTwo patients, brother and sister, suffering from congenital afibrinogenemia are reported. This condition has previously not been described from Scandinavia. Both suffered from severe umbilical hemorrhage soon after birth and a continuing bleeding tendency.
S, OSEID, H M, SVENDSEN
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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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Congenital afibrinogenemia [PDF]
The Journal of Pediatrics, 1957 Burton J. Grossman, Robert E. Carter
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