Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/76045
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dc.contributor.authorMarti-Herrero, Men_US
dc.contributor.authorCabrera-Lopez, JCen_US
dc.contributor.authorToledo, Len_US
dc.contributor.authorPerez-Candela, Ven_US
dc.contributor.authorBonnet, Den_US
dc.date.accessioned2020-11-26T11:17:21Z-
dc.date.available2020-11-26T11:17:21Z-
dc.date.issued1998en_US
dc.identifier.issn0210-0010en_US
dc.identifier.otherWoS-
dc.identifier.urihttp://hdl.handle.net/10553/76045-
dc.description.abstractIntroduction. Moebius's syndrome is an entity present at birth, characterized by oculofacial paralysis and external ophthalmoplegia. Other cranial nerves can also be affected and associated to skeletal abnormalities and neurologic symptoms. It appears sporadically sometimes of familiar nature, presenting special facies with total absence of facial expression and severe strabismus. The pathogenesis of the syndrome still remains unknown, being the transitory situation of fetal hypoxia/ischemic the most accepted theory. In some cases chromosomal abnormalities have been detected. Clinical case. We reported three children with different symptoms, two of them are siblings whose father is affected bur he was not diagnosed until adult age. Conclusions. We conclude pointing out the different presentation of the disease, the appearance in several members of a family and its chronically evolution.en_US
dc.languageengen_US
dc.relation.ispartofRevista de Neurologiaen_US
dc.sourceRevista De Neurologia [ISSN 0210-0010], v. 27 (160), p. 975-978, (Diciembre 1998)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320507 Neurologíaen_US
dc.subject320711 Neuropatologíaen_US
dc.subject.otherCranial Nerves Paralysisen_US
dc.subject.otherMoebius'S Syndromeen_US
dc.subject.otherSpecial Faciesen_US
dc.titleMoebius' syndrome. Three different forms of presentationen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.33588/rn.27160.98066en_US
dc.identifier.scopus0032240789-
dc.identifier.isi000078278100013-
dc.contributor.authorscopusid56636191600-
dc.contributor.authorscopusid6602314344-
dc.contributor.authorscopusid7003557555-
dc.contributor.authorscopusid6603056985-
dc.contributor.authorscopusid57196577719-
dc.description.lastpage978en_US
dc.identifier.issue160-
dc.description.firstpage975en_US
dc.relation.volume27en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid5559920-
dc.contributor.daisngid4652421-
dc.contributor.daisngid6139195-
dc.contributor.daisngid2721255-
dc.contributor.daisngid4114077-
dc.description.numberofpages4en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Marti-Herrero, M-
dc.contributor.wosstandardWOS:Cabrera-Lopez, JC-
dc.contributor.wosstandardWOS:Toledo, L-
dc.contributor.wosstandardWOS:Perez-Candela, V-
dc.contributor.wosstandardWOS:Bonnet, D-
dc.date.coverdateDiciembre 1998en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.scieSCIE
item.fulltextSin texto completo-
item.grantfulltextnone-
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