Marmara Üniversitesi Açık Arşiv Sistemi

Oral manifestation and dental management of catch 22 syndrome

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dc.contributor.author Kulan, Pınar
dc.contributor.author Pekiner, Filiz Namdar
dc.contributor.author Akyüz, Serap
dc.date.accessioned 2014-07-25T12:02:56Z
dc.date.available 2014-07-25T12:02:56Z
dc.date.issued 2013
dc.identifier.issn 2147-7957
dc.identifier.uri http://hdl.handle.net/11424/1994
dc.description.abstract The deletion of chromosome 22q11.2 is described as CATCH 22, Velocardiofacial Syndrome or Di George Syndrome. The acronym of CATCH 22 stands for cardiac defect, abnormal faces, thymic hypoplasia, cleft palate, hypocalcaemia but the acronym does not express all of the symptoms of CATCH 22 syndrome. Some clinical findings of CATCH 22 relate to congenital cardiac defects, velopharyngeal insufficiency with or without cleft palate, immune problems, feeding difficulties, hypocalcaemia, learning disabilities, behavioral abnormalities and lastly characteristic facial features. A treatment protocol of a 7-year-old child with CATCH 22 syndrome who also has dental caries complaint, toothache has been presented. Dental caries treatment and prophylactic application have been done for the patient. As a result, this study basically depicts how a dental approach can be followed for those patients who have CATCH 22 syndrome. en_US
dc.language.iso en en_US
dc.publisher Marmara Dental Journal en_US
dc.subject CATCH 22 syndrome, FISH, thymic hypoplasia en_US
dc.title Oral manifestation and dental management of catch 22 syndrome en_US
dc.type Article en_US
dc.contributor.authorID TR48153
dc.contributor.authorID
dc.contributor.authorID


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