Nivo II – Ekstpertske obuke
Modul 2
Etiologija autizma i komorbidna stanja
- Epidemiologija autizma
- Faktori rizika
- Genetika autizma
- Neurobiološki osnovi autizna
- Autizam I komorbiditeti
- Razumevanje i objašnjenje menjanja epidemiologije poremećaja iz spektra autizma.
- Razumevanje kompleksne interakcije između genetskih i faktora rizika okruženja.
- Znanje o glavnim genetskim i neurobiološkim eksplanatornim modelima poremećaja iz spektra autizma.
- Opisivanje i interpretiranje najčešćih komorbidnih stanja povezanih sa autizmom.
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- DSM-5 criteria
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- http://hdl.handle.net/11245/1.532127
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- Moreno-De Luca, D. et al. (2012). Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts. Mol. Psychiatry 18, 1090–1095.
- Parellada, M., et al. (2014). The neurobiology of autism spectrum disorders. European Psychiatry, 29(1), 11-19.
- Phelan, K. & McDermid, H. E. (2012). The 22q13.3 deletion syndrome (Phelan–McDermid syndrome). Mol. Syndromol. 2, 186–201.
- Radoeva, P.D., et al. (2014). Association between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypes. Psychiatr Genet 24:269-272.
- Veltman, M.W., et al. (2005). Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review. Psychiatr Genet 15: 243-254.
- Vorstman, J. A., et al. (2017). Autism genetics: opportunities and challenges for clinical translation. Nature Reviews Genetics.
- Woodman, A. C., et al. (2016). Trajectories of internalizing and externalizing symptoms among adults with autism spectrum disorders. Development and Psychopathology, 28(2), 565-581.
- https://ec.europa.eu/health/major_chronic_diseases/diseases/autistic_en#fragment1
- https://ec.europa.eu/health/sites/health/files/major_chronic_diseases/docs/asds_eu_en.pdf
Smatra se da je polaznik uspešno prešao modul ukoliko na testu ima barem 75% tačnih odgovora.