Familial Parry-Romberg disease

被引：28
作者：
Anderson, PJ
Molony, D
Haan, E
David, DJ
机构：
[1] Womens & Childrens Hosp, Australian Craniofacial Unit, Adelaide, SA 5006, Australia
[2] Womens & Childrens Hosp, Dept Clin Genet, Adelaide, SA 5006, Australia
[3] Univ Adelaide, Australian Craniofacial Inst, Adelaide, SA 5006, Australia
来源：
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY | 2005年 / 69卷 / 05期
关键词：
Parry-Romberg disease; face; hemifacial atrophy;
D O I：
10.1016/j.ijporl.2004.12.004
中图分类号：
R76 [耳鼻咽喉科学];
学科分类号：
100213 ;
摘要：
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. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码：705 / 708
页数：4
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