Orodental findings in Hallermann-Streiff syndrome.

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dc.contributor.authorParikh, Shilpa
dc.contributor.authorGupta, Swati
dc.date.accessioned2012-08-09T06:20:13Z
dc.date.available2012-08-09T06:20:13Z
dc.date.issued2012-01
dc.description.abstractHallermann-Streiff syndrome-also called occulomandibulofacial syndrome, Francois syndrome, oculomandibulodyscephaly with hypotrichosis, Aubry syndrome I, and Ullrich-Fremery-Dohna syndrome-is a rare genetic disorder, which comprisesmultiple congenital abnormalities affecting chiefly the head and face. It is characterized by bird-like facies, dental abnormalities, hypotrichosis, atrophy of skin, congenital cataracts, bilateral microphthalmia, and proportionate nanism. An interesting case of Hallermann-Streiff syndrome in a 23-year-old female patient is reported here, with the emphasis on the orodental findings.en_US
dc.identifier.citationParikh Shilpa, Gupta Swati. Orodental findings in Hallermann-Streiff syndrome. Indian Journal of Dental Research. 2012 Jan-Feb; 23(1): 124.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/140201
dc.language.isoenen_US
dc.source.urihttps://www.ijdr.in/article.asp?issn=0970-9290;year=2012;volume=23;issue=1;spage=124;epage=124;aulast=Parikhen_US
dc.subjectCongenital abnormalitiesen_US
dc.subjectHallermann-Streiff syndromeen_US
dc.subjectorodental findingsen_US
dc.subject.meshDental Caries --pathology
dc.subject.meshDental Enamel Hypoplasia --pathology
dc.subject.meshFacies
dc.subject.meshFemale
dc.subject.meshHallermann's Syndrome --pathology
dc.subject.meshHumans
dc.subject.meshMandible --abnormalities
dc.subject.meshSyndactyly --pathology
dc.subject.meshTemporal Bone --abnormalities
dc.subject.meshTemporomandibular Joint --abnormalities
dc.subject.meshTooth Abnormalities --pathology
dc.subject.meshYoung Adult
dc.titleOrodental findings in Hallermann-Streiff syndrome.en_US
dc.typeArticleen_US
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