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.identifier.uri	http://repository.limu.edu.ly/handle/123456789/1114
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.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

Except where otherwise noted, this item's license is described as Attribution 3.0 United States