| Literature DB >> 15850693 |
Peter J Anderson1, Darren Molony, Eric Haan, 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.Entities:
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Year: 2005 PMID： 15850693 DOI： 10.1016/j.ijporl.2004.12.004
Source DB: PubMed Journal: Int J Pediatr Otorhinolaryngol ISSN： 0165-5876 Impact factor: 1.675