Results 151 to 160 of about 1,912 (211)

[Clinical phenotypes and genotypes of congenital fibrinogen disorder: an analysis of 16 children]. [PDF]

open access: yesZhongguo Dang Dai Er Ke Za Zhi
Wang M   +7 more
europepmc   +1 more source

Congenital afibrinogenemia. A case report and therapeutic trials

open access: yesThe Turkish Journal of Pediatrics, 1966
S Ozsoylu, C Altay, B Corbacioğlu
doaj  

Congenital afibrinogenemia

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.
H, al-Mondhiry, W C, Ehmann
exaly   +3 more sources

CONGENITAL AFIBRINOGENEMIA

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
openaire   +2 more sources

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