Indian Journal of Dental Research (Jan 2012)

Orodental findings in Hallermann-Streiff syndrome

  • Shilpa Parikh,
  • Swati Gupta

DOI
https://doi.org/10.4103/0970-9290.99063
Journal volume & issue
Vol. 23, no. 1
pp. 124 – 124

Abstract

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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.

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