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Dental Features of William Syndrome

dc.contributor.authorAlbackoush, Zainab
dc.descriptionWilliams 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 problemsen_US
dc.publisherfaculty of Basic Medical Science - Libyan International Medical Universityen_US
dc.rightsAttribution 3.0 United States*
dc.titleDental Features of William Syndromeen_US

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