Results 201 to 210 of about 8,625 (250)

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 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, S, Gomber, N, Madan, U, Rusia, S, Sharma   +4 more
openaire   +2 more sources

Thromboembolism in Congenital Factor VII Deficiency

Acta Haematologica, 2009
An Israeli family of Persian origin was investigated for factor VII deficiency. The proposita, derived from a consanguineous marriage, had repeated thrombophlebitis attacks, pulmonary embolism and rectal bleeding. The family studied and the proposita had low factor VII procoagulant activity and low factor VII antigen.
T, Shifter, I, Machtey, D, Creter
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Factor VII Congenital Deficiency

Haemostasis, 2009
In congenital factor VII deficiency the clinical picture is related to the levels of factor VII coagulant activity; when factor VΠ:C levels are very low the bleeding episodes can occur frequently. The most frequent bleedings are menorrhagia and metrorrhagia in females and hemarthrosis in both sexes.
G. Mariani, M.G. Mazzucconi
openaire   +1 more source

Japanese family with congenital factor VII deficiency

Pediatrics International, 2015
AbstractCongenital factor VII (FVII) deficiency is a rare bleeding disorder with autosomal recessive inheritance. The present female patient was diagnosed with congenital FVII deficiency because of low hepaplastin test (HPT), although vitamin K was given. Heterozygous p.A191T mutation was detected in the peripheral blood, and the same mutation was also
Kanae, Sakakibara, Yoshiki, Okayama, Kenji, Fukushima, Shunsaku, Kaji, Michiko, Muraoka, Yujiro, Arao, Akira, Shimada   +6 more
openaire   +2 more sources

Pregnancy in women with congenital factor VII deficiency

Haemophilia, 2006
Summary.  The aim was to review the pregnancy and obstetric outcome in women with factor VII (FVII) deficiency. The study group contained women with FVII deficiency, registered with Haemophilia centre and Haemostasis Unit at the Royal Free Hospital, London. The women were interviewed and case notes were reviewed.
A A, Kulkarni, C A, Lee, R A, Kadir
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

Congenital Factor VII Deficiency

2018
Coagulation factor (F) II (prothrombin) is a vitamin K-dependent coagulation factor which has an essential role in coagulation cascade. This protein is activated to thrombin by Factor X in the presence of FV and calcium. Congenital FII deficiency is an autosomal recessive bleeding disorder with an estimated incidence of 1:2,000,000 worldwide.
Mahmood Shams, Akbar Dorgalaleh
openaire   +1 more source

Carrier detection in factor VII congenital deficiency

British Journal of Haematology, 1985
SummaryThirty obligate and 28 possible carriers of factor VII congenital deficiency, belonging to 16 families, were studied in relation to the immunological variants to which the kindreds belonged, namely, VII+, VIIR and VII‐. Factor VII activity and antigen determinations in these subjects formed two phenotypical patterns: a discrepant pattern ...
G. Mariani, J. Hermans, M. Orlando, M. G. Mazzucconi, N. Ciavarella, A. Faiella, M. Berrettini, A. Chistolini, G. D. Di Nucci, P. M. Mannucci, F. Mandelli   +10 more
openaire   +3 more sources

Prostate surgery in severe congenital factor VII deficiency: A case report [PDF]

Urology Case Reports, 2019
Moussa M, Abou Chakra M.
exaly   +2 more sources