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hemophilia a/حمى

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الصفحة 1 من عند 66 النتائج

Dengue fever in a patient with severe haemophilia: a case report.

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BACKGROUND Dengue fever is the most rapidly spreading mosquito-borne viral disease in the world. Haemophilia A is the commonest inherited bleeding disorder. There is little data on the incidence and outcome of dengue in patients with haemophila. We report a case of a patient with severe haemophila

MANAGEMENT OF SPLENECTOMY IN HAEMOPHILIA: CASE OF SPONTANEOUS RUPTURE OF SPLEEN DUE TO GLANDULAR FEVER IN A HAEMOPHILIAC.

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[Nodular and cavitary pneumocystosis in a patient with hemophilia A and the acquired immunodeficiency syndrome].

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A 25-year-old man with hemophilia A who had received concentrated plasma and plasma factor VIII products since childhood presented with a productive cough and a fever. The CD4/CD8 ratio of peripheral lymphocyte subsets was very low and the serum was positive for anti-HIV antibodies. The chest

Mild hemophilia A presaged by recurrent postoperative hemorrhagic complications in an elderly patient.

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BACKGROUND Mild hemophilia without spontaneous bleeding can remain undiagnosed for a lifetime. However, intracranial hemorrhage is one of the most serious complications for patients with hemophilia. In addition, hemorrhagic complications after emergency surgery tend to arise from

Pharmacokinetic study of recombinant human factor IX in previously treated patients with hemophilia B in Taiwan.

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OBJECTIVE The pharmacokinetic (PK) study of recombinant human factor IX (rFIX) has been done in patients with hemophilia B in areas other than Taiwan. However, wide patient-related variability in recovery is noted and there is no PK study of rFIX in Taiwanese patients with hemophilia B. The purpose

Emergency department utilization by haemophilia patients in United States.

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BACKGROUND Patients with haemophilia are prone to medical emergencies. Emergency departments (ED) often do not have a haematologist on-call for consultation. OBJECTIVE The aim of this study was to determine the utilization of ED by patients with haemophilia. METHODS Retrospective review of the

Bleeding events and safety outcomes in persons with haemophilia A with inhibitors: A prospective, multi-centre, non-interventional study.

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BACKGROUND Prospectively collected, real-world data on bleeds, haemophilic treatment and safety outcomes in persons with haemophilia A (PwHA) with factor VIII (FVIII) inhibitors are limited. A prospective, global, multi-centre, non-interventional study (NIS; NCT02476942) collected detailed

[Sulfamethoxazole-trimethoprim-induced pneumonitis in a patient with hemophilia B who was infected with the human immunodeficiency virus].

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Severe cellular immunosuppression developed in a 25-year-old man with hemophilia B who was infected with the human immunodeficiency virus (HIV). Four days after administration of sulfamethoxazole-trimethoprim (SMX-TMP) for prophylaxis against Pneumocystis carinii pneumonia (PCP), diffuse uptake of

[Severe parvovirus B19 infection in an immunocompetent child with hemophilia A].

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BACKGROUND B19 parvovirus is a widespread virus whose typical manifestations in immunocompetent children are erythema infectiosum, acute erythroblastopenia and fetal anemia. METHODS An 11 year-old immunocompetent patient with hemophilia A was referred for an hemorrhagic syndrome. Forty days after a

HIV transmission to patients with hemophilia by heat-treated, donor-screened factor concentrate.

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Six hemophilia patients previously seronegative for human immunodeficiency virus (HIV) seroconverted between September 1986 and September 1987. None had risk factors for HIV infection other than hemophilia. We compared the factor concentrates received by these patients with the concentrates received

Management of human immunodeficiency virus-induced thrombocytopenia in hemophilia.

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Three patients with severe hemophilia and Human Immunodeficiency Virus (HIV) infection seropositive for virus antibody, presented with thrombocytopenia. Treatment with prednisolone, danazol (in one patient) and intravenous gammaglobulin, produced only transient responses. In one case, danazol

Septic arthritis in children with hemophilia.

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Four of the 139 children with hemophilia followed up at our center have developed septic arthritis during the past 6 years (2.9% incidence). Two infections were caused by Streptococcus pneumoniae and one each by Staphylococcus aureus and Haemophilus influenzae type B. Common features at time of

Acute cardiac tamponade due to spontaneous bleeding in a child with haemophilia A.

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In severe haemophilia A, patients, start from the first years of life, with spontaneous bleeding and require transfusion. However, cardiac tamponade due to spontaneous pericardial bleeding is rare. An 11-year-old boy receiving haemophilia A treatment was referred to the Department of Paediatric

Hemophilia a and spinal epidural hematoma in children.

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Hemophilia A is an X-linked bleeding disorder, caused by deficient or defective blood coagulation factor VIII. The most characteristic symptoms of the severe forms of hemophilia A are joint and muscle bleeds. Intracranial hemorrhage occurs only in 3-10% of the patients. Spinal epidural hematomas are

[The differential diagnosis of hemarthrosis--septic arthritis in patients with hemophilia].

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A 12-year-old boy with severe hemophilia A fell ill with high fever and painful swelling of joints. There was a delay of four days in the diagnosis of septic arthritis. The course of the disease shows some important distinguishing criteria, speaking in favour of septic arthritis: 1. longlasting
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