Parikh, ShilpaGupta, Swati2012-08-092012-08-092012-01Parikh Shilpa, Gupta Swati. Orodental findings in Hallermann-Streiff syndrome. Indian Journal of Dental Research. 2012 Jan-Feb; 23(1): 124.http://imsear.searo.who.int/handle/123456789/140201Hallermann-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.enCongenital abnormalitiesHallermann-Streiff syndromeorodental findingsDental Caries --pathologyDental Enamel Hypoplasia --pathologyFaciesFemaleHallermann's Syndrome --pathologyHumansMandible --abnormalitiesSyndactyly --pathologyTemporal Bone --abnormalitiesTemporomandibular Joint --abnormalitiesTooth Abnormalities --pathologyYoung AdultArticle