Dental Features of William Syndrome
| dc.contributor.author | Albackoush, Zainab | |
| dc.date.accessioned | 2019-08-07T09:23:04Z | |
| dc.date.available | 2019-08-07T09:23:04Z | |
| dc.date.issued | 2019-03-18 | |
| dc.description | Williams syndrome is a multisystemic rare genetic disorder that was first described in 1961, by a cardiologist from New Zealand. Williams syndrome is caused by a deletion of 26–28 genes in the long arm of chromosome 7 at 7q11.23. The deletion occurs at the time of conception. It is characterized by a number of developmental and physical abnormalities including congenital cardiovascular abnormalities, mental retardation, neurological features, growth deficiency, genitourinary manifestations, gastrointestinal problems, musculoskeletal problems, unique behavioral characteristics, and dental problems | en_US |
| dc.identifier.uri | http://repository.limu.edu.ly/handle/123456789/1114 | |
| dc.language.iso | en | en_US |
| dc.publisher | faculty of Basic Medical Science - Libyan International Medical University | en_US |
| dc.rights | Attribution 3.0 United States | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/3.0/us/ | * |
| dc.title | Dental Features of William Syndrome | en_US |
| dc.type | Other | en_US |