Results 201 to 210 of about 29,955 (251)
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Factor VII deficiency

American Journal of Hematology, 1981
AbstractThis report describes three patients with factor (F) VII deficiency: two adult siblings and an unrelated 5½‐month‐old child who succumbed after several central nervous system (CNS) hemorrhages. This event prompted a review of the literature concerning the incidence and characteristics of intracranial hemorrhage in congenital F VII deficiency.Of
M V Ragni, Jessica H Lewis, Ute Hasiba
exaly   +3 more sources

Factor VII deficiency and its treatment in delivery with recombinant factor VII

European Journal of Obstetrics, Gynecology and Reproductive Biology, 2004
The authors present two cases of pregnant women with coagulation disorders--one with inherited deficiency of factor VII and the second with chronic hepatitis. Both cases were successfully treated with recombinant activated factor VII of coagulation (NovoSeven) in delivery. The advantages of using this product are discussed.
B, Pehlivanov, N, Milchev, G, Kroumov
exaly   +3 more sources

Congenital factor VII deficiency

The Journal of Pediatrics, 1971
Summary A case of factor VII deficiency in a PuertoRican boy is described. He presented with epistaxis as the only symptom. The importance of early diagnosis of the defect is stressed. Identification of heterozygous carriers is also of importance because these persons, for unknown reasons, might present with hemorrhagic diathesis.
M L, Falter, M F, Kaufman
openaire   +2 more sources

Congenital factor VII deficiency

The Indian Journal of Pediatrics, 2004
A 1(1/2)-month-old baby with seizures, lethargy and refusal of feeds was diagnosed to have intracranial hemorrhage due to factor VII deficiency. MRI also demonstrated the unusual presence of a hemorrhagic infarct. The case underscores the importance of carrying out neuroimaging and appropriate hematological studies even in the absence of obvious ...
Jagruti P, Sanghvi   +3 more
openaire   +2 more sources

Acquired and Isolated Deficiencies in Factor VII

Clinical Laboratory, 2022
Acquired and isolated deficiencies in FVII are exceptional. They have mainly been reported during states of severe sepsis by the presence of proteases destroying the factor or neoplastic pathologies by the presence of an inhibitor. Consequently, very few cases have been published.We report two cases of isolated and acquired deficiency of factor VII due
F Z, Alouhmy   +3 more
openaire   +2 more sources

Congenital deficiency of factor VII

The Indian Journal of Pediatrics, 1996
A case of congenital factor VII deficiency in a five-year-old child is reported. The patient, born of a non-consanguineous marriage, presented with repeated bouts of epistaxis since childhood. The prothrombin time (PT) was markedly prolonged with a normal bleeding time (BT), partial thromboplastin time with Kaolin (PTTK) and platelet count. The patient
M, Sikka   +4 more
openaire   +2 more sources

Factor VII deficiency and pregnancy

International Journal of Gynecology & Obstetrics, 1989
Hereditary factor VII deficiency is very rare in pregnancy (one in 500,000). However, obstetricians should consider this diagnosis whenever the prothrombin time is prolonged while the activated partial thromboplastin time is normal. The factor VII level increases in normal pregnancy, but the effect of pregnancy upon the factor VII level in deficient ...
H E, Fadel, J S, Krauss
openaire   +2 more sources

Hereditary Factor‐VII Deficiency in the Beagle

British Journal of Haematology, 1972
Summary. Hereditary factor‐VII deficiency is identified in another large colony of beagles. Evidence is presented to suggest that this trait may be relatively widespread in colonies in Great Britain.
N W, Spurling   +3 more
openaire   +2 more sources

CONGENITAL DEFICIENCY OF FACTOR VII

Australasian Annals of Medicine, 1958
SummaryLaboratory investigations are described in a female patient who suffers from a congenital hæmorrhagic disorder due to deficiency of Factor VII. The one‐stage prothrombin time using brain extract was greatly prolonged, but using viper venom was normal. All tests of the intrinsic blood coagulation mechanism, including the thromboplastin generation
openaire   +2 more sources

Hobby-Induced Factor VII Deficiency

Pathophysiology of Haemostasis and Thrombosis, 2009
Hemorrhagíc tendency and granulocytopenia due to prolonged contact with trichloroethylene and toluene are described in a boy whose hobby was model air-plane assembly. The hemostatic defects found were hypoproconvertinemia, moderate hypofibrinogenemia, and increased capillary fragility.
J, Pinkhas   +3 more
openaire   +2 more sources

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