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dc.contributor.authorM. Biria
dc.contributor.authorB. Nazemi
dc.contributor.authorF. Akbari
dc.contributor.authorA. Rahmati
dc.date.accessioned2017-09-18T10:48:07Z
dc.date.available2017-09-18T10:48:07Z
dc.date.issued2015-12-01
dc.identifier.urihttp://dsp.sbmu.ac.ir/xmlui/handle/123456789/66974
dc.description.abstractBACKGROUND: Freeman-Sheldon syndrome is a rare hereditary disorder characterised by three basic abnormalities, namely microstomia, camptodactyly with ulnar deviation of the fingers, and clubfoot. The majority of these patients have microstomia and dental crowding, making oral hygiene difficult and increasing the risk of caries. Treatment of these patients requires a coordinated effort by a team of specialists, including a paediatrician, an anaesthesiologist, a plastic surgeon, a paediatric dentist, and an orthodontist. Herein, we describe dental problems of a child with Freeman-Sheldon syndrome and the treatment procedures performed.
dc.sourceEuropean journal of paediatric dentistry : official journal of European Academy of Paediatric Dentistry
dc.titleFreeman-Sheldon syndrome: a case report
dc.journal.volume16
dc.journal.issue4
dc.journal.pages311-314
dc.contributor.authorid37040484800
dc.contributor.authorid57101046000
dc.contributor.authorid56998525000
dc.contributor.authorid57192803575
dc.contributor.citation37040484800|60018934|M. Biria
dc.contributor.citation57101046000|60012874|B. Nazemi
dc.contributor.citation56998525000|60018934|F. Akbari
dc.contributor.citation57192803575|60018934|A. Rahmati
dc.contributor.affiliationid60018934
dc.contributor.affiliationid60012874
dc.contributor.affiliationid60018934
dc.contributor.affiliationid60018934


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