Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12188/22082| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Pop-Jordanova Nada | en_US |
| dc.contributor.author | Zorcec, Tatjana | en_US |
| dc.date.accessioned | 2022-08-10T11:28:17Z | - |
| dc.date.available | 2022-08-10T11:28:17Z | - |
| dc.date.issued | 2018 | - |
| dc.identifier.uri | http://hdl.handle.net/20.500.12188/22082 | - |
| dc.description.abstract | Neurodevelopmental disorders with or without autism can be inherited and impose a genetic evaluation, especially when more members of a family are involved. In this article we report the case of two siblings who came for the first time to our attention at the age of 2, 6 years for a global neurodevelopmental delay associated with an autism spectrum disorder. CGH-array analysis showed the same characteristics in both, 16p.13.11-p12.3 duplication inherited by the father. Our results correspond to other, published in literature. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | WJAHR | en_US |
| dc.relation.ispartof | World journal of advance healthcare research | en_US |
| dc.subject | neurodevelopmental delay | en_US |
| dc.subject | autism | en_US |
| dc.subject | genes | en_US |
| dc.title | TWO SIBLINGS WITH NEURODEVELOPMENT DELAY AND AUTISTIC BEHAVIOR WITH THE SAME GENETIC MUTATION | en_US |
| dc.type | Article | en_US |
| item.fulltext | With Fulltext | - |
| item.grantfulltext | open | - |
| crisitem.author.dept | Faculty of Medicine | - |
| Appears in Collections: | Faculty of Medicine: Journal Articles | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Two siblings WJAHR.pdf | 372.51 kB | Adobe PDF | View/Open |
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