Disease definition. Hallermann-Streiff syndrome is a rare genetic syndrome characterized mainly by head and facial abnormalities such as bird-like facies ( with. Hallermann-Streiff syndrome is characterized by a typical skull shape ( brachycephaly with frontal bossing), hypotrichosis, microphthalmia, cataracts, beaked. Hallermann-Streiff syndrome (HSS) is a rare inherited disorder characterized by malformations of the cranium and facial bones, congenital.
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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 year-old female patient is reported strelff, with the emphasis on the orodental findings.
Congenital abnormalities, Hallermann-Streiff syndrome, orodental findings. None, Conflict of Interest: This article has been cited by 1 Generalized odontodysplasia in a 5-year-old patient with Hallermann-Streiff syndrome: Orodental findings in Hallermann-Streiff syndrome.
How to cite this article: Parikh S, Gupta S. Indian J Dent Res ; How to cite this URL: The typical bird-like facies and parrot-beak nose, sparse hairs, hypertelorism, and strabismus Click here to view.
Hallermann Streiff Syndrome-The Oral Manifestations in a Child | OMICS International
Yellowish discoloration of teeth, with microdontia and extensivecarious involvement Click here to view. Panoramic view depict the dental findings. Hypoplastic condyles and fossa, flat articular eminence, and flattened mandible can be seen Click here to view.
TMJ tomograph shows the relationship of the articulating surfaces of the TMJ hypoplastic condyles and fossa, flat articular eminence in open and closed position Click here to view. Hand-wrist radiographs reveal bilateral syndactyly involving the 4 th and 5 th digits, with complete soft tissue fusion and bony fusion at the distal phalanges Click here to view.
Radiograph of pelvis shows dysplastic pubic bone and pubic dilatation. Mild cortical irregularity of the left pubic bone is seen.
Hallermann Streiff Syndrome-The Oral Manifestations in a Child
Click here to view. A case report from Turkey.
Obstructive sleep apnoea in a puerperal patient with Hallermann-Streiff syndrome. Eur Respir J ; Craniodentofacial manifestations in Hallermann-Streiff syndrome. Syndromes of the head and neck 2 nd Ed: New York City, U. J Bone Joint Surg Am ; Br J Ophthal ; This article has been cited by. Generalized odontodysplasia in a 5-year-old patient with Hallermann-Streiff syndrome: Related articles Congenital abnormalities Hallermann-Streiff syndrome orodental findings.