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American Journal of Ophthalmology
Volume 145, Issue 6
, Pages 997-1001.e1
, June 2008
The Value of Keratometry and Central Corneal Thickness Measurements in the Clinical Diagnosis of Marfan Syndrome
References
- Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene. Nature. 1991;352:337–339
- . Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils. J Cell Biol. 1986;103:2499–2509
- . A comparative histologic study of the fibrillin microfibrillar system in the lens capsule of normal subjects and subjects with Marfan syndrome. Invest Ophthalmol Vis Sci. 1998;39:84–93
- . Microfibril abnormalities of the lens capsule in patients with Marfan syndrome and ectopia lentis. Ophthalmic Genet. 2000;21:9–15
- Immunohistochemical localization of fibrillin in human ocular tissues (Relevance to the Marfan syndrome). Arch Ophthalmol. 1995;113:103–109
- . Revised diagnostic criteria for the Marfan syndrome. Am J Med Genet. 1996;62:417–426
- . Dural ectasia is a common feature of the Marfan syndrome. Am J Hum Genet. 1988;43:726–732
- . The eye in the Marfan syndrome. Trans Am Ophthalmol Soc. 1981;79:684–733
- . Presenting signs and clinical diagnosis in individuals referred to rule out Marfan syndrome. Ophthalmic Genet. 2003;24:35–39
- . Cornea in Marfan disease: Orbscan and in vivo confocal microscopy analysis. Invest Ophthalmol Vis Sci. 2002;43:1757–1764
PII: S0002-9394(08)00090-1
doi: 10.1016/j.ajo.2008.01.028
© 2008 Elsevier Inc. All rights reserved.
« Previous
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American Journal of Ophthalmology
Volume 145, Issue 6
, Pages 997-1001.e1
, June 2008
