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dc.contributor.authorТрајковски, Владимирen_US
dc.date.accessioned2018-11-23T14:51:53Z-
dc.date.available2018-11-23T14:51:53Z-
dc.date.issued1999-
dc.identifier.citationТрајковски, Владимир (1999). Генетски аспекти на глувоста. Годишен зборник на Филозофскиот факултет 52, 423-435en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12188/870-
dc.description.abstractThe deafness means a total losing sense of hearing or hearing's damage which make impossible the social contact. It can be aquired and congenital. The statistics data show that from all factors that cause the deafness about 10% are well know genetic syndroms, 20% are familiar forms etiological insufficiently explain; to the group so called criptogen deafness belong about 30% with unknown etiology and about 40% are aquired. The hearing's damage is caused by genetic and enviroumental reasons. Monogenetic diseases followed by losing a hearing are grouped in ten main groups. In the genetic counselings today giving genetic informations and paying attention more to posterity of risky families, including the early rehabilitation of deaf children still plays main role in preventives of deafness.en_US
dc.language.isomken_US
dc.publisherФилозофски факултет, Скопјеen_US
dc.relation.ispartofГодишен зборник на Филозофскиот факултет / Annuaire de la Faculté de Philosophieen_US
dc.subjectглувост, генетски, синдроми, болестиen_US
dc.titleГенетски аспекти на глувостаen_US
dc.title.alternativeGenetic aspects of deafnessen_US
dc.typeJournal Articleen_US
item.fulltextWith Fulltext-
item.grantfulltextopen-
crisitem.author.deptFaculty of Philosophy-
Appears in Collections:Faculty of Philosophy 04: Journal Articles / Статии во научни списанија
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