Hallermann Streiff Syndrome-The Oral Manifestations in a ChildSonu Acharya1*, Mamta Mohanty2 and Sheetal Acharya3
- *Corresponding Author:
- Sonu Acharya
Institute of Dental sciences, SOA University
Bhubaneswar, Odisha, India
E-mail: [email protected]
Received date: July 30, 2015; Accepted date:August 31, 2015; Published date: September 07, 2015
Citation: Acharya S, Mohanty M, Acharya S (2015) Hallermann Streiff Syndrome-The Oral Manifestations in a Child. J Genet Syndr Gene Ther 6:268. doi:10.4172/2157-7412.1000268
Copyright: © 2015 Acharya S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Hallermann-Streiff syndrome (HSS) is a rare genetic disorder that is primarily characterized by distinctive malformations of the skull and facial region, sparse hair, eye abnormalities, dental defects, atrophic skin changes and a proportionate short stature. Here we discuss a case of 9 years-old female child who presented with abnormal facial features, dental problems and associated cardiac problems.