Search for dissertations about: "fetal genotyping"
Showing result 1 - 5 of 7 swedish dissertations containing the words fetal genotyping.
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1. Fetal and neonatal alloimmune thrombocytopenia : immunological mechanisms and clinical consequences
Abstract : Fetal and neonatal alloimmune thrombocytopenia (FNAIT) is a rare condition that may occur in connection with pregnancy, when maternal antibodies directed against paternally inherited platelet antigens cross the placenta and mediate thrombocytopenia in the fetus and neonate. FNAIT puts the fetus at risk of severe bleedings, with an intracranial hemorrhage being the most feared outcome. READ MORE
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2. New strategies to prevent fetal and neonatal complications in Rhesus D immunization
Abstract : The general purpose of this thesis was to investigate if fetal and neonatal complications due to RhD immunization in the mother could be prevented by 1) reducing procedure-related complications in intrauterine blood transfusions and by 2) reducing the incidence of RhD immunization by providing routine antenatal anti-D prophylaxis during pregnancy selectively to non-immunized RhD negative women with RhD positive fetuses. Paper I was a retrospective study including 284 intrauterine transfusions in 84 women 1990-2010. READ MORE
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3. Factor V Leiden mutation and pregnancy. Haemostasis during pregnancy in non-carriers and carriers of factor V Leiden mutation, with special emphasis on placenta-mediated and venous thromboembolic complications and on blood coagulation and fibrinolysis markers for prediction of complications
Abstract : Factor V Leiden (FVL) mutation elevates the risk of venous thromboembolism (VTE) in general. During pregnancy, the haemostatic balance is changed in the direction of hypercoagulability, resulting in an increased incidence of VTE. 42 women were followed longitudinally during pregnancy and the puerperium. READ MORE
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4. Metabolic and cognitive effects after early prenatal dexamethasone treatment
Abstract : Congenital adrenal hyperplasia (CAH), due to 21-hydroxylase deficiency (21OHD), is a disease with an inborn error of the adrenal steroid synthesis. This enzyme deficiency leads to cortisol shortage and androgen excess. READ MORE
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5. Hypospadias : analysis of a complex genetic disorder
Abstract : BACKGROUND: Hypospadias is a common inborn error of the male urethra that involves an abnormally placed urethral opening. Its complex etiology is largely elusive to date. Twin and familial studies highlight a genetic background in hypospadias. Environmental factors have also been identified, particularly the exposure to endocrine disrupters. READ MORE