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https://hdl.handle.net/2440/55879
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Type: | Journal article |
Title: | Familial Parry-Romberg disease |
Author: | Anderson, P. Molony, D. Haan, E. David, D. |
Citation: | International Journal of Pediatric Otorhinolaryngology, 2005; 69(5):705-708 |
Publisher: | Elsevier Sci Ireland Ltd |
Issue Date: | 2005 |
ISSN: | 0165-5876 1872-8464 |
Statement of Responsibility: | Peter J. Anderson, Darren Molony, Eric Haan and David J. David |
Abstract: | Parry–Romberg disease (or hemifacial atrophy) is a rare condition affecting the face. It commences in childhood but its aetiology remains unknown, and is sporadic. Two cases are presented who were biological first cousins. We believe that this is the first recorded example of this condition occurring in family members. |
Keywords: | Parry–Romberg disease Face Hemifacial atrophy |
DOI: | 10.1016/j.ijporl.2004.12.004 |
Description (link): | http://www.elsevier.com/wps/find/journaldescription.cws_home/506038/description#description |
Published version: | http://dx.doi.org/10.1016/j.ijporl.2004.12.004 |
Appears in Collections: | Aurora harvest Dentistry publications |
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