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Familial Parry-Romberg disease.

作者信息

Anderson Peter J, Molony Darren, Haan Eric, David David J

机构信息

Australian Craniofacial Unit, Women's and Children's Hospital, SA, Australia.

出版信息

Int J Pediatr Otorhinolaryngol. 2005 May;69(5):705-8. doi: 10.1016/j.ijporl.2004.12.004.

DOI:10.1016/j.ijporl.2004.12.004
PMID:15850693
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.

摘要

相似文献

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