dc.contributor.author | Lubinus Badillo, Federico | spa |
dc.contributor.author | Castilla Pinilla, Campo E | spa |
dc.date.accessioned | 2020-10-27T14:22:16Z | |
dc.date.available | 2020-10-27T14:22:16Z | |
dc.date.issued | 2003-08-08 | |
dc.identifier.issn | 2382-4603 | |
dc.identifier.issn | 0123-7047 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12749/10515 | |
dc.description.abstract | Se presentan dos casos de displasia septoóotica o Síndrome de Morsier, una entidad del sistema nervioso que sólo se puede confirmar por medio de neuroimágenes. Estas consisten en ausencia de septum pellucidum, agenesia de cuerpo calloso, atrofia cerebelosa, porencefalia, dilatación ventricular y lipomas o quistes cerebrales, junto con neurohipófisis ectópica, aplásica o hipoplásica. El cuadro clínico es variable, dependiendo del grado de compro-miso del nervio óptico, la función hipotalamica y las alteraciones asociadas. El pronóstico en general es bueno. [Lubinus F, Castillo CE. Displasia septoóptica (Sindrome de Morsier). | spa |
dc.format.mimetype | application/pdf | spa |
dc.language.iso | spa | spa |
dc.publisher | Universidad Autónoma de Bucaramanga UNAB | |
dc.relation | https://revistas.unab.edu.co/index.php/medunab/article/view/260/243 | |
dc.relation.uri | https://revistas.unab.edu.co/index.php/medunab/article/view/260 | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/2.5/co/ | |
dc.source | MedUNAB; Vol. 6 Núm. 17 (2003): Especial Pediatría; 98-101 | |
dc.subject | Ciencias biomédicas | |
dc.subject | Ciencias de la vida | |
dc.subject | Innovaciones en salud | |
dc.subject | Investigaciones | |
dc.title | Displacia septoóptica (Sindrome de Morsier) | spa |
dc.title.translated | Septo-optic dysplasia (Morsier syndrome) | eng |
dc.publisher.faculty | Facultad Ciencias de la Salud | spa |
dc.publisher.program | Pregrado Medicina | spa |
dc.type.driver | info:eu-repo/semantics/article | |
dc.type.local | Artículo | spa |
dc.type.coar | http://purl.org/coar/resource_type/c_6501 | |
dc.subject.keywords | Health Sciences | eng |
dc.subject.keywords | Medicine | eng |
dc.subject.keywords | Medical Sciences | eng |
dc.subject.keywords | Biomedical Sciences | eng |
dc.subject.keywords | Life Sciences | eng |
dc.subject.keywords | Innovations in health | eng |
dc.subject.keywords | Research | eng |
dc.subject.keywords | Septo-optic dysplasia | eng |
dc.subject.keywords | Morsier syndrome | eng |
dc.subject.keywords | Agenesis of the corpus callosum | eng |
dc.identifier.instname | instname:Universidad Autónoma de Bucaramanga UNAB | spa |
dc.type.hasversion | Info:eu-repo/semantics/publishedVersion | |
dc.type.hasversion | info:eu-repo/semantics/acceptedVersion | spa |
dc.rights.accessrights | info:eu-repo/semantics/openAccess | spa |
dc.relation.references | Barkovich AJ. Pediatric neuroimagin. Phyladelphia, Raven Press 1995: 236-8 | spa |
dc.relation.references | De Morsier G. Etudes sur les dysraphies, cranioencéfaliques III. Agénésie du septum pallucidum avec malformation du tra-cus optique. La displásie septo-optiqué. Schweiz Arch Neurol Psychiatr 1956; 77:267-92 | spa |
dc.relation.references | Benner JD, Presla MW, Gratz E, Joslyn J, Schwartz M, Kelman S. Septo optic dysplasia in two siblings. Am J Ophthal 1990; 109:632-7 | spa |
dc.relation.references | Mitchell Q, Zacharin MR, Scheffer E. Ectopic posterior pituitary lobe and periventricular heterotopia: cerebral malformations with the same underlying mechanism? Am J Neuroradiol 2002; 23:1475-81 | spa |
dc.relation.references | Lubinsky S. Septooptic dysplasia is a vascular disrupcion se-cuence. Am J Med Genetics 1997; 9:235- 6. | spa |
dc.relation.references | Willnow S, Kiess W, Butenandt O, Dorr HG, Ender A, Strasser-Vogel B, et al. Endocrine disorders in septo optic dysplasia (De Morsier syndrome) – evaluation and follow up of 18 patients. Eur J Pediatr 1996;155:179-84 | spa |
dc.relation.references | Martínez-Sánchez L, Arce A, Caritg-Bosch J, Campistol J, Pavia, Gean Molins E. Displasia septoóptica. Rev Neurol 2002; 35:439-42 | spa |
dc.relation.references | Lan KY, Tam W, Lam PKL, Wood BP. Septo optic dysplasia. Am J Dis Child 1993; 147:71-2 | spa |
dc.relation.references | Cameron FJ, Khadilkar VV, Stanhope R. Pituitary disfunction, morbidity and mortality with congenital midline malformation of the cerebrum. Eur J Pediatr 1999; 158:97-102 | spa |
dc.relation.references | De Morsier HD. Hypoplasia of the pituitary and adrenal cortex. JPediatr 1956;48:633 | spa |
dc.relation.references | Sheehan AG, Martin SR, Stephure D, Scott RB. Neonatal cholesthasis, hypoglycemia and congenital hypopituitarism. J Pediatr Gastroenterol Nutr 1992; 14: 426-30 | spa |
dc.relation.references | Sener-R. Septo-optic dysplasia associated with cerebral cortical dysplasia (cortico-septo-optic dysplasia). J Neuroradiol 1996; 23:245-7 | spa |
dc.relation.references | Miller SP, Shevel MI, Patenaude Y, Poulin C, O ́Gorman AM. Septo-optic dysplasia plus: A spectrum of malformations of cortical development. Neurology 2000; 54:1701-3 | spa |
dc.relation.references | Sener R. Septo-optic dysplasia (de Morsier’s syndrome) associated with total callosal absence. A new type of the anomaly. J Neuroradiol 1996; 23:79-81 | spa |
dc.relation.references | Gilbert JD, Scott G, Byard RW. Septo optic dysplasia and unexpected adult death – an autopsy approach. J Forensic Sci 2001; 46:913- | spa |
dc.relation.references | Brodsky MC, Conte FA, Taylor D. Sudden death in septo-optic dysplasia :Report of 5 cases. Arch Opthal 1997; 115:66-70 | spa |
dc.subject.lemb | Ciencias médicas | spa |
dc.subject.lemb | Ciencias de la salud | spa |
dc.subject.lemb | Medicina | spa |
dc.identifier.repourl | repourl:https://repository.unab.edu.co | |
dc.description.abstractenglish | Two cases of septootic dysplasia or Morsier Syndrome are presented, an entity of the nervous system that can only be confirmed through neuroimaging. These consist of absence of septum pellucidum, agenesis of the corpus callosum, cerebellar atrophy, porencephaly, ventricular dilation and cerebral lipomas or cysts, together with ectopic, aplastic or hypoplastic neurohypophysis. The clinical picture is variable, depending on the degree of optic nerve involvement, hypothalamic function and associated alterations. The general prognosis is good. [Lubinus F, Castillo CE. Septo-optic dysplasia (Morsier syndrome). | eng |
dc.subject.proposal | Displasia septoóptica | spa |
dc.subject.proposal | Síndrome de Morsier | spa |
dc.subject.proposal | Agenesia del cuerpo calloso | spa |
dc.type.redcol | http://purl.org/redcol/resource_type/ART | |