Sökning: "fetal anomalies"
Visar resultat 6 - 10 av 10 avhandlingar innehållade orden fetal anomalies.
6. Smoking and pregnancy : with special reference to preterm birth and the feto-placental unit
Sammanfattning : Objective: To study maternal smoking in pregnancy in relation to preterm birth, placental abruption and perinatal mortality in pregnancies with placental abruption, and to pulse wave characteristics in fetal aorta. Methods: Two cohort studies with data on single births obtained from the Swedish Medical Birth Registry (N=311 977 and N=795 459, respectively). LÄS MER
7. Considering a Baby? Responsible Screening for the Future : Ethical and social implications for implementation and use of preconception expanded carrier screening in Sweden
Sammanfattning : Preconception expanded carrier screening is a novel technology that involves the offer of a screening test for many recessive diseases (via an expanded screening panel) to prospective parents, with no priori risk. Test positive couples have a number of reproductive choices; prenatal diagnosis and aborting affected fetus, IVF and preimplantation genetic diagnosis, sperm or ovum donation or simply accept the risk. LÄS MER
8. Role of ion and water channels for lung growth in congenital diaphragmatic hernia
Sammanfattning : Early lung development is based on a continuous cross-talk of growth and transcription factors between the developing lung bud and the surrounding parenchyma. Throughout fetal life, pulmonary growth and differentiation depend on Cl- driven lung liquid secretion. LÄS MER
9. Clinical and molecular genetic characterization of congenital malformations
Sammanfattning : Congenital malformations are important causes of perinatal mortality and morbidity, and around 4% of children are diagnosed with a malformation during their first year of life. Despite improved surgical treatment, several malformations are associated with lifelong sequelae requiring specialized health care. LÄS MER
10. Ear and hearing problems in Turner syndrome
Sammanfattning : Turner Syndrome is a common chromosomal disorder and affects approximately one in every 2000 newborn girl. The syndrome is defined as a total (45,X) or partial loss of the second sex chromosome in combination with the typical characteristic features, which are short stature (less than 150 cm), absent estrogen production due to ovarian dysgenesis, with failure to enter puberty spontaneously and infertility. LÄS MER