Læknablaðið : fylgirit - 01.05.2002, Blaðsíða 25

Læknablaðið : fylgirit - 01.05.2002, Blaðsíða 25
ABSTRACTS / 33RD SNC & 2ND SCNN fied. There are FHM families not linked to either chromosome 19 or 1 and thus at least a third gene locus exists. Heterogeneity is also very likely for the more common entities, migraine with and without aura. The female preponderance of mig- raine could suggest involvement of X-chromosome. Indeed, Nyholt and colleagues have found, in two large multigenerational migraine pedigrees, significant excess allele sharing of Xq in typical familial migraine. Peroutka and colleagues reported overrepresentation of DRD2 IC allele of the D2 dopamine receptor gene (in chromo- some 11) among patients with migraine with aura. In Sardinia, Del Zompo and colleagues demonstrated a positive association bet- ween allele 1 of the same dopamine receptor gene in migraineurs with both jawning and nausea during allacks. Dopaminergic candi- date genes have thus also been in the spotlight. Tlie CACNAIA gene has been connected also to migraine with and without aura in association analyses. Further evidence was demonstrated by Ter- windt and colleagues, who found increased allele sharing in the region in affected siblingpairs, especially in pairs with migraine with aura. Recently even more genomic areas have been studied. Nyholt and colleagues linked typical migraine in an Australian family to chromosome 19pl3 with evidence for genetic heterogeneity. An insuline receptor gene on 19pl3.3/2 and an endothelin type A receptor gene are among the hot new topics. Lea and collegues have found linkage and association to lq31 in 83 Australian pedi- grees. Most recently, in 50 extensive Finnish migraine families, Wessman and collegues found susceptibility locus for nonhemi- plegic migraine with aura on chromosome 4q24. These novel dis- coveries clearly underly the complexity and heterogeneity of mig- raine with and without aura. L19 - Botulinum toxin treatment from the clinician’s point of view Jakobsson F Dept. of Neurology, Landspítali University Hospital Grensás, Reykjavík, Iceland Abstract not received. L20 - Botulinum toxin and hyperhidrosis. Naver H, Aquilonius S-M Department of Neuroscience, Neurology, Uppsala University Hospital Sweden In 1822 Justus Kerner described muscular paralysis as well as anhid- rosis in botulism. (Kerners disease). In 1996 treatment of focal hyperhidrosis with botulinum toxin was developed in Uppsala, and since 1997 the therapy has replaced sympathectomy for severe palmar hyperhidrosis. The anhidrotic effect lasts long as compared to the effect on dystonia, side effects are minor and transient. For axillary hyperhidrosis the safety and efficacy of btx has been confirmed in two multicentre double blind placebo controlled studies. Frey syndrome and secondary and primary hyperhidrosis at other locations may be treated with similar good results Our demonstration that the severely reduced quality of life of hyperhidrotic patients can be restored, that side effects are transient, that the therapy can be performed by nurses, motivates that the therapy should be offered these patients before sympathectomy. L22 - Epidemiology of epilepsy in lceland Ólafsson E Dept. of Neurology, Landspítali University Hospital Hringbraut, Reykjavík, Iceland Abstract not received. L23 - Risk factors for epilepsy Hauser A Dept. of Neurology, Columbia University, New York, USA Abstract not received. L24 - Living with eating difficulties after stroke. Nursing assessment and interventions. Jacobsson C Department of Nursing, Umeá University, Sweden The need to eat and drink is something we all have in common and this makes food an important element in our lives. Food is con- sumed not only for the nourishment of the body, but it also nourishes the heart, mind and soul. Food and food habits are integral parts of the culture and an aspect of existence associated with for instance lifestyles. Eating special kinds of food and drinking special kinds of beverages reflect social and cultural identities and are intimately related to concepts of self and identity. Cultural food practices have symbolic meanings that people may use to express themselves and communicate. In general, food and eating are symbols of interpersonal acceptance, friendliness, sociability and communion. The meal is a time to unite in fellowship and create a sense of belonging and it is intimately connected with emotions. Cultural rules and learnt habits are important for our experience of meaning in eating. When eating with other people, we are required to follow cultural rules about how to behave and to show table manners. Food can be treated as a code, meaning that the messages it encodes will be found in the social relations which are expressed in the social structure. The relationship between cultural pattern and nutrition is central to an understanding of human life. In nursing care, it is therefore important to pay more attention to cultural values and nutrition in recovery from illness as well as the promotion of wellbeing. Literature about living with stroke indicates that recovery is closely related to activities that matter to the patients and that the patients’ life situations are influenced primarily by their own way of dealing with their disabilities. The bodily breakdown may lead to identity confusion, the feeling of unreality and the awareness of a changed role in life. The bodily changes may result in both physical and psychological trauma, which could be best described as personal catastrophes. Eating difficulty is described as related to chewing, swallowing, loss of lip control, drooling, and leakage of food from the mouth and is of special interest in nursing care. This may have serious physical as well as social consequences and is reported to be stress- ful and to result in anxiety, shame, loneliness, isolation and lack of appetite. Research findings show that these eating difficulties cause inadequate food intake, aspiration and malnutrition. Malnutrition Læknablaðið/Fylgirit 43 2002/88 25
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