Publication
Reed's Syndrome
| dc.contributor.author | Almeida, FT | |
| dc.contributor.author | Santos, R P | |
| dc.contributor.author | Carvalho, SD | |
| dc.contributor.author | Brito, C | |
| dc.date.accessioned | 2018-07-06T10:45:14Z | |
| dc.date.available | 2018-07-06T10:45:14Z | |
| dc.date.issued | 2018 | |
| dc.description.abstract | Multiple cutaneous and uterine leiomyomatosis (MCUL), also known as Reed's syndrome, is a rare genodermatosis, with an autosomal dominant pattern of inheritance. It results from a germline heterozygous mutation of fumarate hydratase gene, that is classified as a tumor suppressor gene. Hereditary leiomyomatosis and renal cell cancer is characterized by the association of MCUL with renal cell carcinoma. We report a case of a 57-year-old woman, with multiple cutaneous leiomyomas as the presenting sign of Reed's syndrome. | pt_PT |
| dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
| dc.identifier.citation | Indian J Dermatol. 2018 May-Jun;63(3):261-263. | pt_PT |
| dc.identifier.doi | 10.4103/ijd.IJD_69_18 | pt_PT |
| dc.identifier.uri | http://hdl.handle.net/10400.23/1265 | |
| dc.language.iso | eng | pt_PT |
| dc.peerreviewed | yes | pt_PT |
| dc.subject | Leiomiomatose | pt_PT |
| dc.subject | Síndromes Neoplásicas Hereditárias | pt_PT |
| dc.subject | Neoplasias da Pele | pt_PT |
| dc.subject | Neoplasias Uterinas | pt_PT |
| dc.title | Reed's Syndrome | pt_PT |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| oaire.citation.issue | 3 | pt_PT |
| oaire.citation.startPage | 261-263 | pt_PT |
| oaire.citation.volume | 63 | pt_PT |
| rcaap.rights | openAccess | pt_PT |
| rcaap.type | article | pt_PT |