Coagulation defect of congenital tyrosinaemia.
نویسندگان
چکیده
منابع مشابه
Case Report: Congenital Defect of the Liver Falciform Ligament
Congenital variations and anomalies in the human body are clinically important and surgeons must be aware of those. Various human congenital malformation types have been reported. The liver is the largest organ of the digestive system. Numerous studies surveyed malposition in the liver and its attachments, because variations in the hypochondriac region and liver attachments may cause acute abdo...
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A 6-week-old infant is presented who suffered from a congenital haemorrhagic disorder which caused death from subdural haemorrhage following mild trauma. Haematological investigation revealed deficiencies of factor VII and Christmas factor. Prower-Stuart factor was probably also deficient although investigation of this clotting factor was carried out only on serum obtained at necropsy.
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The association of the presence of an abnormal serum protein fraction between P and y globulins in reticuloendothelial disease and lymphatic leukaemia is a Ml recognized phenomenon (Rundles et al., 1954; Buffa and Rappaport, 1957; Owen e* 1959). The combination of leukaemia and amyloidosis is also recognized, but he presence of a coagulation defect in amyloidosis must be relatively uncommon. CA...
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The importance of non-prothrombin plasma and serum constituents in the physiological conversion of prothrombin to thrombin has been recognized only recently. A hemorrhagic disorder, called "parahemophilia" (Owren's disease), is associated with an elevated prothrombin time attributable to deficiency of a plasma component termed "Factor V" (1, 2). Inadequacy of plasma Ac-globulin, required for ra...
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Clinical and experimental observations are described that indicate that intra-articular fibrinogenolysis is a cause of the defect of coagulation seen when blood is extravasated into a synovial joint.
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ژورنال
عنوان ژورنال: Archives of Disease in Childhood
سال: 1984
ISSN: 0003-9888,1468-2044
DOI: 10.1136/adc.59.11.1088