https://scholars.lib.ntu.edu.tw/handle/123456789/434995
標題: | Haberland syndrome | 作者: | CHIH-CHIEH CHAN JAU-SHIUH CHEN CHIA-YU CHU |
公開日期: | 2005 | 卷: | 23 | 期: | 1 | 起(迄)頁: | 41-45 | 來源出版物: | Dermatologica Sinica | 摘要: | Haberland syndrome, also known as encephalocraniocutaneous lipomatosis (ECCL) is a very rare congenital disorder which has been reported in only 36 cases worldwide since its first description. The syndrome is characterized by several specific clinical findings in different organ systems which can be presented within a spectrum. In our case, the exact diagnosis of ECCL was delayed for 25 years since his birth. We reported this rare case and reviewed related literature. |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-15244343842&partnerID=40&md5=545739c11bad746adcd853b131a80105 https://scholars.lib.ntu.edu.tw/handle/123456789/434995 |
ISSN: | 1027-8117 | SDG/關鍵字: | adult; case report; clinical feature; encephalocraniocutaneous lipomatosis; Haberland syndrome; human; human tissue; lipomatosis; male; rare disease; review; Taiwan |
顯示於: | 醫學系 |
在 IR 系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。