Ocular manifestations and surgical results in patients with Marfan syndrome;Okuläre manifestationen und chirurgische ergebnisse beim Marfan-syndrom

Ophthalmologe

Volumn 103, Issue 9, 2006, Pages 777-782

  Ladewig, M S ^a,b   Robinson, P N ^b   Neumann, L M ^b   Holz, F G ^a   Foerster, M H ^b  

^a UNIVERSITY OF BONN   (Germany)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

Ectopia lentis; Eye; Fibrillin fbn1; Ghent nosology; Marfan syndrome

Indexed keywords

AMBLYOPIA; ARTICLE; CILIARY DISK; CLINICAL ARTICLE; CONTROLLED STUDY; ECTOPIA LENTIS; FIBER; HUMAN; LENS IMPLANT; LENS SUBLUXATION; MARFAN SYNDROME; RETINA DETACHMENT; SECONDARY GLAUCOMA; VITRECTOMY;

ADOLESCENT; ADULT; AGED; CHILD; CHILD, PRESCHOOL; EYE DISEASES; FEMALE; HUMANS; MALE; MARFAN SYNDROME; MIDDLE AGED; OPHTHALMOLOGIC SURGICAL PROCEDURES; RETROSPECTIVE STUDIES; TREATMENT OUTCOME; VISION DISORDERS; VISUAL ACUITY;

EID: 33748790995     PISSN: 0941293X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00347-006-1386-8     Document Type: Article

References (18)

1. Ashworth JL, Murphy G, Rock MJ et al. (1999) Fibrillin degradation by matrix metalloproteinases: implications for connective tissue remodelling. Biochem J 340: 171-181
2. Behki R, Noel LP, Clarke WN (1990) Limbal lensectomy in the management of ectopia lentis in children. Arch Ophthalmol 108: 809-811
3. Boegner F (1914) Über zwei Fälle von Arachnodaktylie. Z Kinderheilkd 12: 160-184
4. Booms P, Pregla R, Ney A et al. (2005) RGD-containing fibrillin-1 fragments upregulate matrix metalloproteinase expression in cell culture: a potential factor in the pathogenesis of the Marfan syndrome. Hum Genet 116: 51-61
5. Cross HE, Jensen AD (1973) Ocular manifestations in the Marfan syndrome and homocystinuria. Am J Ophthalmol 75: 405-420
6. Farnsworth PN, Burke P, Dotto ME, Cinotti AA (1977) Ultrastructural abnormalities in a Marfan's syndrome lens. Arch Ophthalmol 95: 1601-1606
7. Jarrett WH (1967) Dislocation of the lens. A study of 166 hospitalized cases. Arch Ophthalmol 78: 289-296
8. Kielty CM, Davies SJ, Phillips JE (1995) Marfan syndrome: fibrillin expression and microfibrillar abnormalities in a family with predominant ocular defects. J Med Genet 32: 1-6
9. Klüppel M, Sundmacher R, Althaus C (1997) Surgical management of Marfan-associated and idiopathic lens dislocations. Ophthalmologe 94: 739-744
10. Lipscomb KJ, Clayton-Smith J, Harris R (1997) Evolving phenotype of Marfan's syndrome. Arch Dis Child 76: 41-46
11. Maumenee IH (1981) The eye in the Marfan syndrome. Trans Am Ophthalmol Soc 79: 684-733
12. Mir S, Wheatley HM, Hussels IE et al. (1998) 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 39: 84-93
13. Nelson LB, Maumenee IH (1982) Ectopia lentis. Surv Ophthalmol 27: 143-160
14. Paepe A de, Devereux RB, Dietz HC et al. (1996) Revised diagnostic criteria for the Marfan syndrome. Am J Med Genet 62: 417-426
15. Pessier AP, Potter KA (1996) Ocular pathology in bovine Marfan's syndrome with demonstration of altered fibrillin immunoreactivity in explanted ciliary body cells. Lab Invest 75: 87-95
16. Raghunath M, Nienaber C, Kodolitsch Y (1997) 100 Jahre Marfan-Syndrom - eine Bestandsaufnahme. Dtsch Ärztebl 94 13: 656-662
17. Robinson PN, Godfrey M (2000) The molecular genetics of Marfan syndrome and related microfibrillopathies. J Med Genet 37: 9-25
18. Robinson PN, Godfrey M (eds) (2004) The Marfan syndrome: a primer for clinicians and scientists. Landes Bioscience/Eurekahcom, Kluwer Academic/Plenum Publishers