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Clinical manifestations and oral findings in fraser syndrome

dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorDiniz, Michele Baffi
dc.creatorLima, Luciana Monti
dc.creatorSacono, Nancy Tomoko
dc.creatorDe Paula, Andréia Bolzan
dc.creatorSantos-Pinto, Lourdes Aparecida Martins dos
dc.date2014-05-27T11:22:34Z
dc.date2016-10-25T18:24:16Z
dc.date2014-05-27T11:22:34Z
dc.date2016-10-25T18:24:16Z
dc.date2007-09-01
dc.date.accessioned2017-04-06T01:26:20Z
dc.date.available2017-04-06T01:26:20Z
dc.identifierJournal of Dentistry for Children, v. 74, n. 3, p. 231-235, 2007.
dc.identifier1551-8949
dc.identifier1935-5068
dc.identifierhttp://hdl.handle.net/11449/69861
dc.identifierhttp://acervodigital.unesp.br/handle/11449/69861
dc.identifier2-s2.0-47949113498
dc.identifier0000-0003-2386-842X
dc.identifierhttp://www.ingentaconnect.com/content/aapd/jodc/2007/00000074/00000003/art00015
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/891038
dc.descriptionThis article is the first known case report of Fraser syndrome in the dental literature. Its purpose was to present the clinical manifestations, oral findings, and dental treatment of a 14-year, 10-month-old female patient. Fraser syndrome is a rare recessive autosomal genetic disorder characterized by multisystemic malformation, usually comprising cryptophthalmos, syndactyly, and renal defects. The child presented with: (1) hydrocephaly; (2) face asymmetry; (3) low-inserted ears; (4) flat nose bridge; (5) cryptophthalmos; (6) bilateral absence of eyeballs; (7) hypertelorism; (8) syndactyly on the left fingers and toes; (9) skeletal defects; and (10) lower limb asymmetry. The intraoral examination revealed: (1) complete primary denture; (2) malocclusion; (3) tooth crowding; (4) ogival palate; (5) normal labial frena; (6) absence of lingual frenum (not compromising the tongue movements); (7) parched lips; (8) supragingival calculus adhered to all tooth surfaces; and (9) moderate gingivitis. The dental treatment consisted of periodic monitoring of the patient's oral health status and supragingival scaling associated with topical applications of 0.12% chlorhexidine digluconate gel at 2-week intervals to reduce gingivitis.
dc.languageeng
dc.relationJournal of Dentistry for Children
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectFraser syndrome
dc.subjectOral findings
dc.subjectTooth anomalies
dc.subjectcongenital malformation
dc.subjectconsanguinity
dc.subjectdentition
dc.subjecteye malformation
dc.subjectfemale
dc.subjectgingivitis
dc.subjecthard palate
dc.subjecthuman
dc.subjecthypertelorism
dc.subjectmalocclusion
dc.subjectmouth disease
dc.subjectmultiple malformation syndrome
dc.subjectpathology
dc.subjectpreschool child
dc.subjectpreventive dentistry
dc.subjectsyndactyly
dc.subjectsyndrome
dc.subjecttongue
dc.subjecttooth calculus
dc.subjectAbnormalities, Multiple
dc.subjectChild, Preschool
dc.subjectConsanguinity
dc.subjectDental Calculus
dc.subjectDental Scaling
dc.subjectDentition, Primary
dc.subjectEye Abnormalities
dc.subjectFemale
dc.subjectGingivitis
dc.subjectHumans
dc.subjectHypertelorism
dc.subjectLingual Frenum
dc.subjectMalocclusion
dc.subjectMouth Abnormalities
dc.subjectPalate, Hard
dc.subjectSyndactyly
dc.subjectSyndrome
dc.titleClinical manifestations and oral findings in fraser syndrome
dc.typeOtro


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