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Osorio Chacón, Mario Tribín Gómez, Alfonso Hernández Rodríguez, Maria Paula Vanegas Acevedo, Juan José Vidales Correa, Liliana 2006-06-01 00:00:00 2022-02-21T20:36:22Z 2006-06-01 2006-06-01 00:00:00 2022-02-21T20:36:22Z Sociedad de Cirugía de Bogotá, Hospital de San José y Fundación Universitaria de Ciencias de la Salud Fundación Universitaria de Ciencias de la Salud FUCS - 0 info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/4.0/ http://purl.org/coar/access_right/c_abf2 https://revistas.fucsalud.edu.co/index.php/repertorio/article/view/423 síndrome Marfán hallazgos oftalmológicos ectopia lentis Marfan syndrome ophthalmological findings ectopia lentis Manifestaciones oculares del síndrome de marfán Ocular manifestations of marfan syndrome application/pdf Artículo de revista Journal article http://purl.org/coar/resource_type/c_6501 info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Text http://purl.org/coar/version/c_970fb48d4fbd8a85 10.31260/RepertMedCir.v15.n2.2006.423 0121-7372 https://repositorio.fucsalud.edu.co/handle/001/2325 2462-991X https://doi.org/10.31260/RepertMedCir.v15.n2.2006.423 spa • 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. • 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. • 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. • Dean JC. Management of Marfan syndrome. Heart. 2002 Jul;88(1):97-103. • 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. • Krause KJ. Marfan syndrome: literature review of mortality studies. J Insur Med. 2000;32(2):79- 88. • Loja David, Vilca Maricela, Avilés Roberto. Síndrome de Marfan. A propósito de un caso. An. Fac. Med. 2001;62(1) • 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 . • Maumenee IH. The eye in the Marfan syndrome. Trans Am Ophthalmol Soc. 1981;79:684-733. • 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. • 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. • 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. https://revistas.fucsalud.edu.co/index.php/repertorio/article/download/423/478 Núm. 2 , Año 2006 : Abril – Junio 76 2 72 15 Revista Repertorio de Medicina y Cirugía Publicationmetadata.only