Orbscan mapping in Ehlers-Danlos syndrome

Journal of Cataract and Refractive Surgery

Volumn 30, Issue 8, 2004, Pages 1795-1798

  Pesudovs, Konrad ^a,b  

^a Ultralase   (United Kingdom)

^b UNIVERSITY OF BRADFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; ASTIGMATISM; BIOMECHANICS; CASE REPORT; CLINICAL EXAMINATION; CORNEA CURVATURE; CORNEA LIMBUS; CORNEA THICKNESS; DIAGNOSTIC IMAGING; DISEASE CLASSIFICATION; EHLERS DANLOS SYNDROME; EXTRAOCULAR MUSCLE; EYE COLOR; FEMALE; HUMAN; KERATOCONUS; MUSCLE WEAKNESS; MYOPIA; OPHTHALMOPLEGIA; PRIORITY JOURNAL; REFRACTIVE SURGERY; SCLERA; TOPOGRAPHY; TREATMENT CONTRAINDICATION;

ASTIGMATISM; CORNEA; CORNEAL DISEASES; CORNEAL TOPOGRAPHY; EHLERS-DANLOS SYNDROME; FEMALE; HUMANS; KERATOMILEUSIS, LASER IN SITU; MIDDLE AGED; MYOPIA; SCLERAL DISEASES;

EID: 4143149700     PISSN: 08863350     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcrs.2004.05.002     Document Type: Article

References (21)

1. Beighton P., De Paepe A., Steinmann B., et al. Ehlers-Danlos syndromes. Revised nosology, Villefranche, 1997; Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK) Am J Med Genet. 77:1998;31-37
2. Byers P.H. Disorders of collagen biosynthesis and structure. Scriver C.R., Beaudet A.L., Sly W.S., Valle D. The Metabolic and Molecular Bases of Inherited Disease. 8th ed:2001;5241-5284 McGraw-Hill, New York, NY
3. Mao J.-R., Bristow J. The Ehlers-Danlos syndrome. on beyond collagens J Clin Invest. 107:2001;1063-1069
4. Tilstra D.J., Byers P.H. Molecular basis of hereditary disorders of connective tissue. Annu Rev Med. 45:1994;149-163
5. Burrows N.P. The molecular genetics of the Ehlers-Danlos syndrome. Clin Exp Dermatol. 24:1999;99-106
6. Trinkaus-Randall V, Edelhauser HF, Leibowitz HM, Freddo TF. Corneal structure and function. In: Leibowitz HM, Waring GO III, eds, Corneal Disorders; Clinical Diagnosis and Management, 2nd ed. Philadelphia, PA, W B Saunders 1998; 2-31
7. Kuming B.S., Joffe L. Ehlers-Danlos syndrome associated with keratoconus; a case report. S Afr Med J. 52:1977;403-405
8. Beighton P. The Ehlers-Danlos Syndrome. 1970;William Heinemann Medical Books, London
9. Cameron J.A. Corneal abnormalities in Ehlers-Danlos syndrome type VI. Cornea. 12:1993;54-59
10. Moestrup B. Tenuity of cornea with Ehlers-Danlos syndrome. Acta Ophthalmol. 47:1969;704-708
11. Green W.R., Friedman-Kien A., Banfield W.G. Angioid streaks in Ehlers-Danlos syndrome. Arch Ophthalmol. 76:1966;197-204
12. Beighton P. Serious ophthalmological complications in the Ehlers-Danlos syndrome. Br J Ophthalmol. 54:1970;263-268
13. Bossu A., Lambrechts J. Manifestations oculaires du syndrome d'Ehlers-Danlos. Ann Oculist. 187:1954;227-236
14. Robertson I. Keratoconus and the Ehlers-Danlos syndrome. a new aspect of keratoconus Med J Aust. 1:1975;571-573
15. Macsai M.S., Lemley H.L., Schwartz T. Management of oculus fragilis in Ehlers-Danlos type VI. Cornea. 19:2000;104-107
16. May M.A., Beauchamp G.R. Collagen maturation defects in Ehlers-Danlos keratopathy. J Pediatr Ophthalmol Strabismus. 24:1987;78-82
17. Yeowell H.N., Walker L.C. Ehlers-Danlos syndrome type VI results from a nonsense mutation and a splice site-mediated exon-skipping mutation in the lysyl hydroxylase gene. Proc Assoc Am Physicians. 109:1997;383-396
18. Jarisch A., Giunta C., Zielen S., et al. Sibs affected with both Ehlers-Danlos syndrome type VI and cystic fibrosis. Am J Med Genet. 78:1998;455-460
19. Pousi B., Hautala T., Hyland J.C., et al. A compound heterozygote patient with Ehlers-Danlos syndrome type VI has a deletion in one allele and a splicing defect in the other allele of the lysyl hydroxylase gene. Hum Mutat. 11:1998;55-61
20. McDermott M.L., Holladay J., Liu D., et al. Corneal topography in Ehlers-Danlos syndrome. J Cataract Refract Surg. 24:1998;1212-1215
21. Rabinowitz Y.S., McDonnell P.J. Computer-assisted corneal topography in keratoconus. Refract Corneal Surg. 5:1989;400-408