A Clinical Study Of 31 Individuals With Midline Facial Defects With Hypertelorism And A Guideline For Follow-up.

dc.creatorGil-da-Silva-Lopes, Vera Lúcia
dc.creatorMaciel-Guerra, Andréa Trevas
dc.date2007-Jun
dc.date2015-11-27T13:10:20Z
dc.date2015-11-27T13:10:20Z
dc.date.accessioned2018-03-29T01:05:13Z
dc.date.available2018-03-29T01:05:13Z
dc.identifierArquivos De Neuro-psiquiatria. v. 65, n. 2B, p. 396-401, 2007-Jun.
dc.identifier0004-282X
dc.identifier
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/17665003
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/197395
dc.identifier17665003
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1297628
dc.descriptionIn order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) and to etiologic diagnosis of the isolated form, 31 patients with MFDH unaffected by known syndromic associations were evaluated. Group A included patients personally examined by the authors, while Group B included those previously evaluated by other geneticists. Among the 14 patients from Group A, there were 7 with distinct pictures of multiple congenital anomalies. In Group B, 5 of the 17 patients also exhibited a distinct pattern of defects. Among isolated MFDH, there was association with anomalies of the skull and facial bones (13/14), otorhinologic (11/16), central nervous system (9/16), and ocular (6/7), and audiologic (3/16); 1/3 of the cases had a relevant gestational intercurrences. Isolated FNM may have involvement of environmental components in some cases; the possibility of a syndromic picture should be extensive investigated. Follow-up of such patients must include the examinations herein performed.
dc.description65
dc.description396-401
dc.languageeng
dc.relationArquivos De Neuro-psiquiatria
dc.relationArq Neuropsiquiatr
dc.rightsaberto
dc.rights
dc.sourcePubMed
dc.subjectAdolescent
dc.subjectAdult
dc.subjectCerebellar Diseases
dc.subjectCerebellum
dc.subjectChild
dc.subjectChild, Preschool
dc.subjectCraniofacial Abnormalities
dc.subjectFacies
dc.subjectFemale
dc.subjectFollow-up Studies
dc.subjectFrontal Bone
dc.subjectHumans
dc.subjectHypertelorism
dc.subjectInfant
dc.subjectMagnetic Resonance Imaging
dc.subjectMale
dc.subjectNeurologic Examination
dc.subjectTomography, X-ray Computed
dc.titleA Clinical Study Of 31 Individuals With Midline Facial Defects With Hypertelorism And A Guideline For Follow-up.
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución