Manifestaciones oculares del síndrome de marfán

dc.creatorOsorio Chacón, Mario
dc.creatorTribín Gómez, Alfonso
dc.creatorHernández Rodríguez, Maria Paula
dc.creatorVanegas Acevedo, Juan José
dc.creatorVidales Correa, Liliana
dc.date.accessioned2006-06-01 00:00:00
dc.date.accessioned2022-02-21T20:36:22Z
dc.date.accessioned2022-09-27T12:36:48Z
dc.date.available2006-06-01 00:00:00
dc.date.available2022-02-21T20:36:22Z
dc.date.available2022-09-27T12:36:48Z
dc.date.created2006-06-01 00:00:00
dc.date.created2022-02-21T20:36:22Z
dc.date.issued2006-06-01
dc.identifier10.31260/RepertMedCir.v15.n2.2006.423
dc.identifier0121-7372
dc.identifierhttps://repositorio.fucsalud.edu.co/handle/001/2325
dc.identifier2462-991X
dc.identifierhttps://doi.org/10.31260/RepertMedCir.v15.n2.2006.423
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3595802
dc.languagespa
dc.publisherSociedad de Cirugía de Bogotá, Hospital de San José y Fundación Universitaria de Ciencias de la Salud
dc.relation• Ades LC, Holman KJ, Brett MS, Edwards MJ, Bennetts B. Ectopia lentis phenotypes and the FBN1 gene. Am J Med Genet A. 2004 Apr 30;126(3):284-9.
dc.relation• Behan WM, Longman C, Petty RK, Comeglio P, Child AH, Boxer M, et al. Muscle fibrillin deficiency in Marfan's syndrome myopathy. J Neurol Neurosurg Psychiatry. 2003 May;74(5):633-8.
dc.relation• Comeglio P, Evans AL, Brice G, Cooling RJ, Child AH. Identification of FBN1 gene mutations in patients with ectopia lentis and marfanoid habitus. BrJ Ophthalmol. 2002 Dec;86(12):1359- 62.
dc.relation• Dean JC. Management of Marfan syndrome. Heart. 2002 Jul;88(1):97-103.
dc.relation• De Paepe A, Devereux RB, Dietz HC, Hennekam RC, Pyeritz RE. Revised diagnostic criteria for the Marfan syndrome. Am J Med Genet. 1996 Apr 24;62(4):417-26.
dc.relation• Krause KJ. Marfan syndrome: literature review of mortality studies. J Insur Med. 2000;32(2):79- 88.
dc.relation• Loja David, Vilca Maricela, Avilés Roberto. Síndrome de Marfan. A propósito de un caso. An. Fac. Med. 2001;62(1)
dc.relation• Loeys B, Nuytinck L, Delvaux I, De Bie S, De Paepe A. Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome. Arch Intern Med. 2001 Nov 12; 161(20):2447-54 .
dc.relation• Maumenee IH. The eye in the Marfan syndrome. Trans Am Ophthalmol Soc. 1981;79:684-733.
dc.relation• Robinson PN, Booms P, Katzke S, Ladewig M, Neumann L, Palz M, et al. Mutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathies. Hum Mutat. 2002 Sep;20(3):153-61.
dc.relation• Rothe MJ, Grant-Kels JM, Kels BD. Ocular and cutaneous manifestations of heritable disorders of collagen and elastic tissue. Dermatol Clin. 1992 Jul;10(3):591-5.
dc.relation• Traboulsi EI, Whittum-Hudson JA, Mir SH, Maumenee IH. Microfibril abnormalities of the lens capsule in patients with Marfan syndrome and ectopia lentis. Ophthalmic Genet. 2000 Mar;21(1):9-15.
dc.relationhttps://revistas.fucsalud.edu.co/index.php/repertorio/article/download/423/478
dc.relationNúm. 2 , Año 2006 : Abril – Junio
dc.relation76
dc.relation2
dc.relation72
dc.relation15
dc.relationRevista Repertorio de Medicina y Cirugía
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.rightshttp://purl.org/coar/access_right/c_abf2
dc.rightsFundación Universitaria de Ciencias de la Salud FUCS - 0
dc.sourcehttps://revistas.fucsalud.edu.co/index.php/repertorio/article/view/423
dc.subjectsíndrome Marfán
dc.subjecthallazgos oftalmológicos
dc.subjectectopia lentis
dc.subjectMarfan syndrome
dc.subjectophthalmological findings
dc.subjectectopia lentis
dc.titleManifestaciones oculares del síndrome de marfán
dc.typeArtículo de revista
dc.typeJournal article


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