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2017, br. 39, str. 131-136
The role of modern genetic in prevention and diagnosis of rare diseases
(naslov ne postoji na srpskom)
Univerzitet u Kragujevcu, Prirodno-matematički fakultet, Institut za biologiju i ekologiju

e-adresasanjamatic@kg.ac.rs
Projekat:
Simultana bioremedijacija i soilifikacija degradiranih prostora, za očuvanje prirodnih resursa biološki aktivnih supstanci i razvoj i proizvodnju biomaterijala i dijetetskih proizvoda (MPNTR - 43004)
Preklinička ispitivanja bioaktivnih supstanci (MPNTR - 41010)

Sažetak
(ne postoji na srpskom)
In this paper, we deal with the problems encountered by those suffering from rare diseases and their families as well as the recommendations of the Council of Europe related to the activities in this field. It gives an estimate of the current situation in our country and emphasizes the need for adoption and implementation of National Plan/Strategy for rare diseases. Given the frequent dependence existing between these diseases and genetic changes, preventive and diagnostic measures have to be based on the application of modern genetics along with upholding ethical principles.
Reference
*** (2005-2011) Serbian Law on Healthcare. Official Gazette, 107/2005, 72/2009, 88/2010, 99/2010 and 57/2011, Accessed 08 February 2017., in Serbian
*** EUROPLAN: Recommendations for the development of national plans and strategies for rare diseases. Available from: www.europlanproject.eu/_newsite_986987/Resources/docs/2008-2011_2.EUROPLANRecommendation.pdf. Accessed 06 January 2017
*** (2016) Zakon o zdravstvenoj dokumentaciji i evidenciji u oblasti zdravstva. Sl. Glasnik RS, [in Serbian] Accessed 11 January 2017
*** (2015) Law on prevention and diagnostics of genetic diseases: Genetically caused anomalies and rare diseases. Official Gazette of Republic of Serbia, January. [in Serbian] Accessed 24 February 2017
Brambati, B. (2000) Prenatal diagnosis of genetic diseases. European Journal of Obstetrics & Gynecology and Reproductive Biology, 90(2): 165-169
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Medić, B., Divac, N., Stopić, B., Savić-Vujović, K., Glišić, A., Cerovac, N., Stojanović, R., Srebro, D., Prostran, M. (2016) The attitudes of medical students towards rare diseases: A cross-sectional study. Vojnosanitetski pregled, vol. 73, br. 8, str. 703-713
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National Organization for Rare Diseases (NORBS) Available from:
Remuzzi, G., Garattini, S. (2008) Rare diseases: what's next?. Lancet, 371(9629): 1978-1979
Stojanov, Lj., Marjanović, B. (2002) Hiperfenilalaninemije. u: Stojanov Lj. [ur.] Inherited neurometabolic diseases in children, Beograd: Zavod za udžbenike i nastavna sredstva, str. 61-82
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O članku

jezik rada: engleski
vrsta rada: neklasifikovan
DOI: 10.5937/KgJSci1739131S
objavljen u SCIndeksu: 02.11.2017.
Creative Commons License 4.0

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