Publication: Haberland syndrome
| dc.contributor.author | CHIH-CHIEH CHAN | en_US |
| dc.contributor.author | JAU-SHIUH CHEN | en_US |
| dc.contributor.author | CHIA-YU CHU | en_US |
| dc.creator | Chan C.-C.;Chen J.-S.;Chia-Yu Chu | |
| dc.date.accessioned | 2019-12-04T08:44:18Z | |
| dc.date.available | 2019-12-04T08:44:18Z | |
| dc.date.issued | 2005 | |
| dc.description.abstract | 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. | en_US |
| dc.identifier.issn | 1027-8117 | |
| dc.identifier.scopus | 2-s2.0-15244343842 | |
| dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-15244343842&partnerID=40&md5=545739c11bad746adcd853b131a80105 | |
| dc.identifier.uri | https://scholars.lib.ntu.edu.tw/handle/123456789/434995 | |
| dc.language.iso | en | en_US |
| dc.relation.ispartof | Dermatologica Sinica | en_US |
| dc.relation.journalissue | 1 | en_US |
| dc.relation.journalvolume | 23 | en_US |
| dc.relation.pages | 41-45 | en_US |
| dc.subject.classification | [SDGs]SDG3 | |
| dc.subject.other | adult; case report; clinical feature; encephalocraniocutaneous lipomatosis; Haberland syndrome; human; human tissue; lipomatosis; male; rare disease; review; Taiwan | |
| dc.title | Haberland syndrome | en_US |
| dc.type | review | en_US |
| dspace.entity.type | Publication |