dc.creator | Zambelli, H | |
dc.creator | Carelli, E | |
dc.creator | Honorato, D | |
dc.creator | Marba, S | |
dc.creator | Coelho, G | |
dc.creator | Carnevalle, A | |
dc.creator | Iscaife, A | |
dc.creator | da Silva, E | |
dc.creator | Barini, R | |
dc.creator | Sbragia, L | |
dc.date | 2007 | |
dc.date | APR | |
dc.date | 2014-11-16T16:36:58Z | |
dc.date | 2015-11-26T17:25:46Z | |
dc.date | 2014-11-16T16:36:58Z | |
dc.date | 2015-11-26T17:25:46Z | |
dc.date.accessioned | 2018-03-29T00:12:59Z | |
dc.date.available | 2018-03-29T00:12:59Z | |
dc.identifier | Childs Nervous System. Springer, v. 23, n. 4, n. 421, n. 425, 2007. | |
dc.identifier | 0256-7040 | |
dc.identifier | WOS:000244750900010 | |
dc.identifier | 10.1007/s00381-006-0261-x | |
dc.identifier | http://www.repositorio.unicamp.br/jspui/handle/REPOSIP/54994 | |
dc.identifier | http://www.repositorio.unicamp.br/handle/REPOSIP/54994 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/54994 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1284397 | |
dc.description | Prenatal diagnosis of myelomeningocele (MMC) has permitted a better planning for optimum management of the disease. More recently, it has allowed for a possible intrauterine repair of the spinal defect. To describe neurosurgical outcome in children with myelomeningocele and follow-up at a referral center in Fetal Medicine. Patients were characterized for the development of a protocol suitable for fetal surgery, and fetuses who were possible candidates for intrauterine surgery were identified. A retrospective descriptive analysis was performed of 98 cases of fetal myelomeningocele, seen at CAISM-UNICAMP, from January 1994 to December 2002, identifying cases with a possible indication for fetal surgery. Mean gestational age at diagnosis was 29 weeks (17-39); level of lesion was above the sacral region in 92.84%; association with hydrocephalus occurred in 78.57%. During clinical course, 82.5% of patients had neurogenic bladder and 60% had neural and mental deficits. Potential intrauterine repair rate was 11.57%, using criteria from the protocol developed in our service. Myelomeningocele is associated with severe and frequent sequelae. In virtually 12% of our cases, fetal surgery could have been offered as a therapeutic option. | |
dc.description | 23 | |
dc.description | 4 | |
dc.description | 421 | |
dc.description | 425 | |
dc.language | en | |
dc.publisher | Springer | |
dc.publisher | New York | |
dc.publisher | EUA | |
dc.relation | Childs Nervous System | |
dc.relation | Childs Nerv. Syst. | |
dc.rights | fechado | |
dc.rights | http://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0 | |
dc.source | Web of Science | |
dc.subject | prenatal diagnosis | |
dc.subject | myelomeningocele | |
dc.subject | hydrocephalus | |
dc.subject | fetal surgery | |
dc.subject | In-utero | |
dc.subject | Spinal-cord | |
dc.subject | Meningomyelocele | |
dc.subject | Management | |
dc.subject | Repair | |
dc.subject | Bifida | |
dc.subject | Model | |
dc.title | Assessment of neurosurgical outcome in children prenatally diagnosed with myelomeningocele and development of a protocol for fetal surgery to prevent hydrocephalus | |
dc.type | Artículos de revistas | |