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- Title
Orodental findings in Hallermann-Streiff syndrome.
- Authors
Parikh, Shilpa; Gupta, Swati
- Abstract
Hallermann-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.
- Subjects
FACIAL abnormalities; GENETIC disorders; HUMAN abnormalities; MICROPHTHALMIA; CATARACT; SKIN diseases; ATROPHY; GENETICS
- Publication
Indian Journal of Dental Research, 2012, Vol 23, Issue 1, p119
- ISSN
0970-9290
- Publication type
Article
- DOI
10.4103/0970-9290.99063