Syndrome of Hajdu-Cheney: Three Case Reports of Orofacial Interest

Author:

Vingerhoedt E.1,Bailleul-Forestier I.2,Fellus P.3,Schoenaers J.4,Frijns J.-P.5,Carels C.6

Affiliation:

1. Department of Orthodontics, School of Dentistry, Oral Pathology and Maxillo-Facial Surgery, Leuven, Belgium.

2. Centre of Human Genetics, UZ & KU Leuven, Belgium, and Paediatric Dentistry Department, Paris 7 University, Paris, France.

3. Paediatric Stomatology, R. Debré Hospital, AP-HP, France.

4. Department of Maxillo-Facial Surgery, Leuven, Belgium.

5. Center of Human Genetics, Leuven, Belgium.

6. Department of Orthodontics, School of Dentistry, Oral Pathology and Maxillofacial Surgery, KULeuven, Leuven, Belgium.

Abstract

Hajdu-Cheney syndrome is a rare, probably autosomal dominant connective tissue disorder with a variable expressivity. It is characterized by an osteoporotic skeleton, acro-osteolysis, a proportionate short stature, and distinctive orofacial anomalies. The aim of this article is to focus on the orofacial manifestations in two sporadic cases and one familial case with Hajdu-Cheney syndrome. Several common dental and craniofacial features are described. In contrast to earlier proposed diagnostic features, these patients show persisting deciduous teeth, problematic tooth eruption, and tendency toward a Class III malocclusion.

Publisher

SAGE Publications

Subject

Otorhinolaryngology,Oral Surgery

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