Millions of preselected progeny have been born since the development of The Beltsville Sperm Sexing Technology 1986. The method is based on flow cytometry and sorting is done on the basis of DNA difference of the X- and Y-chromosomes. Preselection of progeny provides an opportunity to obtain genetic gain and increased production as well as increased animal welfare and decreased environmental impact. However, the method is associated with low fertility, high costs and uncertainty whether the sorting process contributes to DNA damage and thereby results in genetically impaired progeny. Today, sex sorted sperm is only commercially available in the bovine industry, due to the fact that bull sperm is more suitable for selection than sperm from other species.

Placentan (livmoderkakan) är ett metaboliskt viktigt organ och under opiat och kokain missbruk påverkas placentan negativt och det påverkar fostrets normala utveckling. Syftet med denna litteraturstudie var att ta reda på hur placenta och foster påverkades av opiater och kokain samt om det fanns någon specifik behandling för foster och barn före respektive efter förlossningen. Nio vetenskapliga artiklar granskades och analyserades enligt SBU:s analysmodell. Resultaten visade att acetylkolinfrisättningen och den viktiga aminosyratransporten till fostrets blodomlopp hämmades vid opiat och kokain missbruk. Detta resulterar i tillväxthämning hos fostret som ger lägre födelsevikt, mindre huvudomfång, kortare barn samt att de föds med neonatal abstinens symtom (NAS) i varierande styrka.

The danger and vulnerability associated with a preterm birth seem to be closely correlated with a dysfunction of the fetal hypothalamic-pituitary-adrenal (HPA) axis, whose maturation in the foal is without a doubt as delicate as it is important. Not only is this endocrine cascade vital for the foal in order to cope with neonatal stress, it also appears to be fundamental for the final fetal Intrauterine maturation, as well as for the onset of foaling. Equine gestation exhibits some rather unique features, indicating a somewhat different significance of the endocrine changes associated with HPA maturation, compared to many other species. This hormonal cascade is rapid and confined to a narrow time during late gestation in the horse, and the risk of the foal completely missing it therefore becomes prominent. Induced parturition in the mare may be operated through uterotonic agents, which occasionally bring about premature foals. Desirable seems the ability to initiate equine labour while simultaneously enhancing fetal HPA maturation, as in humans and ruminants through perinatal glucocorticoid administration. However, similar treatment in the horse has resulted in various, sometimes fatal, outcomes. In the light of the distinctive features of equine gestation, difficulties are encountered following such administration of glucocorticoids and ACTH.

Bakgrund: Det finns begränsad kunskap om hur mammor upplever att drabbas av HELLP syndrom och samtidigt mista sitt väntade barn. Ytterligare kunskap kan bidra till ökad förståelse och leda till bättre vård. Syfte: Att beskriva mammors upplevelser av att drabbas av HELLP syndrom och samtidigt mista sitt väntade barn. Metod: En kvalitativ fallstudie med djupintervjuer som analyserades genom kvalitativ innehållsanalys. Resultat: Studien påvisade det kaos och den overklighetskänsla mammorna upplevde då insjuknandet och händelserna skedde i snabb takt.

Renal dysplasia is a developmental anomaly of the kidneys which is considered to be the primary lesion in juvenile progressive nephropathy, a condition leading to chronic renal failure in young dogs. It is defined as disorganised development of the renal parenchyma due to abnormal differentiation, and pathological lesions include persistent foetal structures, dysplastic tubules and cartilaginous and osseus metaplasia. The aetiology of renal dysplasia in dogs is still unknown, but possible causes are infection with canine herpesvirus, teratogenic substances or Intrauterine ureteral obstruction. In some breeds renal dysplasia is a familial or inherited disease. Clinical signs of chronic renal failure, such as polyuria, polydipsia, vomiting, weight loss, anorexia, lethargy and anemia, usually appear before the age of 2 years.