Please use this identifier to cite or link to this item: 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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