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dc.contributor.authorLubinus Badillo, Federicospa
dc.contributor.authorCastilla Pinilla, Campo Espa
dc.date.accessioned2020-10-27T14:22:16Z
dc.date.available2020-10-27T14:22:16Z
dc.date.issued2003-08-08
dc.identifier.issn2382-4603
dc.identifier.issn0123-7047
dc.identifier.urihttp://hdl.handle.net/20.500.12749/10515
dc.description.abstractSe 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.mimetypeapplication/pdfspa
dc.language.isospaspa
dc.publisherUniversidad Autónoma de Bucaramanga UNAB
dc.relationhttps://revistas.unab.edu.co/index.php/medunab/article/view/260/243
dc.relation.urihttps://revistas.unab.edu.co/index.php/medunab/article/view/260
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/
dc.sourceMedUNAB; Vol. 6 Núm. 17 (2003): Especial Pediatría; 98-101
dc.subjectCiencias biomédicas
dc.subjectCiencias de la vida
dc.subjectInnovaciones en salud
dc.subjectInvestigaciones
dc.titleDisplacia septoóptica (Sindrome de Morsier)spa
dc.title.translatedSepto-optic dysplasia (Morsier syndrome)eng
dc.publisher.facultyFacultad Ciencias de la Saludspa
dc.publisher.programPregrado Medicinaspa
dc.type.driverinfo:eu-repo/semantics/article
dc.type.localArtículospa
dc.type.coarhttp://purl.org/coar/resource_type/c_6501
dc.subject.keywordsHealth Scienceseng
dc.subject.keywordsMedicineeng
dc.subject.keywordsMedical Scienceseng
dc.subject.keywordsBiomedical Scienceseng
dc.subject.keywordsLife Scienceseng
dc.subject.keywordsInnovations in healtheng
dc.subject.keywordsResearcheng
dc.subject.keywordsSepto-optic dysplasiaeng
dc.subject.keywordsMorsier syndromeeng
dc.subject.keywordsAgenesis of the corpus callosumeng
dc.identifier.instnameinstname:Universidad Autónoma de Bucaramanga UNABspa
dc.type.hasversionInfo:eu-repo/semantics/publishedVersion
dc.type.hasversioninfo:eu-repo/semantics/acceptedVersionspa
dc.rights.accessrightsinfo:eu-repo/semantics/openAccessspa
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dc.relation.referencesDe 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; 77:267-92spa
dc.relation.referencesBenner JD, Presla MW, Gratz E, Joslyn J, Schwartz M, Kelman S. Septo optic dysplasia in two siblings. Am J Ophthal 1990; 109:632-7spa
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dc.relation.referencesWillnow 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;155:179-84spa
dc.relation.referencesMartínez-Sánchez L, Arce A, Caritg-Bosch J, Campistol J, Pavia, Gean Molins E. Displasia septoóptica. Rev Neurol 2002; 35:439-42spa
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dc.relation.referencesCameron FJ, Khadilkar VV, Stanhope R. Pituitary disfunction, morbidity and mortality with congenital midline malformation of the cerebrum. Eur J Pediatr 1999; 158:97-102spa
dc.relation.referencesDe Morsier HD. Hypoplasia of the pituitary and adrenal cortex. JPediatr 1956;48:633spa
dc.relation.referencesSheehan AG, Martin SR, Stephure D, Scott RB. Neonatal cholesthasis, hypoglycemia and congenital hypopituitarism. J Pediatr Gastroenterol Nutr 1992; 14: 426-30spa
dc.relation.referencesSener-R. Septo-optic dysplasia associated with cerebral cortical dysplasia (cortico-septo-optic dysplasia). J Neuroradiol 1996; 23:245-7spa
dc.relation.referencesMiller SP, Shevel MI, Patenaude Y, Poulin C, O ́Gorman AM. Septo-optic dysplasia plus: A spectrum of malformations of cortical development. Neurology 2000; 54:1701-3spa
dc.relation.referencesSener R. Septo-optic dysplasia (de Morsier’s syndrome) associated with total callosal absence. A new type of the anomaly. J Neuroradiol 1996; 23:79-81spa
dc.relation.referencesGilbert JD, Scott G, Byard RW. Septo optic dysplasia and unexpected adult death – an autopsy approach. J Forensic Sci 2001; 46:913-spa
dc.relation.referencesBrodsky MC, Conte FA, Taylor D. Sudden death in septo-optic dysplasia :Report of 5 cases. Arch Opthal 1997; 115:66-70spa
dc.subject.lembCiencias médicasspa
dc.subject.lembCiencias de la saludspa
dc.subject.lembMedicinaspa
dc.identifier.repourlrepourl:https://repository.unab.edu.co
dc.description.abstractenglishTwo 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.proposalDisplasia septoópticaspa
dc.subject.proposalSíndrome de Morsierspa
dc.subject.proposalAgenesia del cuerpo callosospa
dc.type.redcolhttp://purl.org/redcol/resource_type/ART


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