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Spontaeous capsular ruptures in alport syndrome

  • Original Article
  • Published:
Annals of Ophthalmology

Abstract

Alport syndrome is an inherited disorder affecting the basement membranes, predominantly of the kidneys, eyes, and ears. In our series of 8 patients, anterior lenticonus was the most common ocular feature, as is typical in these cases. However, spontaneous capsular rupture was the presenting feature in 3 patients, rarely reported in Alport syndrome. On follow-up (3 months), all had spontaneous rupture of the lenticonus in the other eye.

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References

  1. Alport AC. Hereditary familial congenital hemorrhagic nephritis. Br Med J. 1927;1:504–506.

    Google Scholar 

  2. Sohar E. Renal disease, inner ear deafness and ocular changes: a new heredofamilial syndrome. Arch Intern Med. 1956;97:627–630.

    CAS  Google Scholar 

  3. Arnott EJ, Crawfurd MD, Toghill PJ. Anterior lenticonus and Alport syndrome. Br J Ophthalmol. 1996;50:390–403.

    Google Scholar 

  4. Nielsen CE. Lenticonus anterior and Alport's syndrome. Acta Ophthalmol. 1978;56:518–530.

    CAS  Google Scholar 

  5. Faggioni R, Scouras J, Streiff EB. Alport's syndrome clinicopathological considerations. Ophthalmologica. 1972;165:1–14.

    Article  PubMed  CAS  Google Scholar 

  6. Govan JAA. Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes? Br J Ophthalmol. 1983;67:493–503.

    PubMed  CAS  Google Scholar 

  7. Ehrlich LH. Spontaneous rupture of lens capsule in anterior lenticonus. Am J Ophthalmol. 1946;29:1274–1281.

    Google Scholar 

  8. Gregg JB, Becker SF. Concomitant progressive deafness, chronic nephritis, and ocular lens disease. Arch Ophthalmol. 1963;69:293–299.

    PubMed  CAS  Google Scholar 

  9. Chavis RM, Grosong T. Corneal arcus in Alport's syndrome. Am J Ophthalmol. 1973;75:793–794.

    PubMed  CAS  Google Scholar 

  10. Teekhasaenee C, Nimmanit S, Wutthipan S, et al. Posterior polymorphous dystrophy and Alport syndrome. Ophthalmology. 1991; 98:1207–1215.

    PubMed  CAS  Google Scholar 

  11. Singh DS, Bisht DB, Kapoor S, Sharma RN, Samkaran K, Majumdar NK. Lenticonus in Alport's syndrome: a family study. Acta Ophthalmol. 1977;55:164–169.

    CAS  Google Scholar 

  12. Brownell RD, Wolter JR. Anterior lenticonus in familial hemorrhagic nephritis. Arch Ophthalmol. 1964;71:481–483.

    PubMed  CAS  Google Scholar 

  13. Mete UO, Karaaslan C, Ozbilgin MK, Polat S, Tap O, Kaya M. Alport's syndrome with bilateral macular hole. Acta Ophthalmol Scand. 1996;74:77–80.

    PubMed  CAS  Google Scholar 

  14. Polack BCP, Hogewind BL. Macular lesions in Alport's disease. Am J Ophthalmol. 1977;84:532–535

    Google Scholar 

  15. Bhatnagar R, Kumar A, Pakrasi S. Alport's syndrome: ocular manifestations and unusual features. Acta Ophthalmol. 1990;68:347–349.

    CAS  Google Scholar 

  16. Chugh KS, Sakhuja V, Agarwal A, et al. Hereditary nephritis (Alport's syndrome): clinical profile and inheritance in 28 kindreds. Nephrol Dial Transplant. 1993;8:690–695.

    PubMed  CAS  Google Scholar 

  17. Razaie-Jami T, KhoshSovour MR, Islami M, et al. Situs inversus: an uncommon extrarenal association of Alport's syndrome. Nephron. 1996;74:426.

    Google Scholar 

  18. Mittal R, Saxena S, Hotchandani RR, Agarwal SK, Tiwari SC, Dash SC. Situs inversus: a rare extrarenal manifestation of Alport's syndrome. Nephron. 1994;68:390.

    PubMed  CAS  Google Scholar 

  19. De-Marchi S, Cecchin E. Asymptomatic autoimmune thyroiditis and thyroid dysfunction in Alport's syndrome: a report of three families. Nephrol Dial Transplant. 1991;6:79–85.

    PubMed  CAS  Google Scholar 

  20. Kashtan CE, Michael AF, Sibley RK, Vernier RL. Hereditary nephritis: Alport syndrome and thin glomerular basement disease. In: Tisher CC, Brenner BM, eds. Renal Pathelogy: With Clinical and Functional Correlations. Vol 2. 2nd ed. Philadelphia, Pa: JB Lippincott; 1994:1239–1266.

    Google Scholar 

  21. Peterson WS, Albert DM. Fundus changes in the hereditary nephropathies. Trans Am Acad Ophthalmol Otolarnyngol. 1974; 78:762–771.

    Google Scholar 

  22. Getisken O, Hendrikse F, Schroder CH, Berden JHM. Retinal abnormalities in Alport's syndrome. Acta Ophthalmol. 1988;66:713–717.

    Article  Google Scholar 

  23. Gehrs KM, Pollock SC, Zilkha G. Clinical features and pathogenesis of Alport retinopathy. Retina. 1995;15:305–311.

    Article  PubMed  CAS  Google Scholar 

  24. Chance JK, Stanley JA. Alport's syndrome: case report and review of ocular manifestations. Ann Ophthalmol. 1977;9:1527–1530.

    PubMed  CAS  Google Scholar 

  25. Jayaprasad B, Satish KR, Chandrashekar N, Upadhyaya NS, Mehta S. Alport's syndrome: a case report. Ind J Ophthalmol. 1994;42:211–212.

    CAS  Google Scholar 

  26. Adler SG, Cohen AH, Gassock RJ. Alport's syndrome In: Brenner BM, ed. Brenner and Rector's The Kidney. 5th ed. Philadelphia, Pa: WB Saunders Co; 1996:1555–1558.

    Google Scholar 

  27. Myers JC, Jones TA, Pohjolainen E, et al. Molecular cloning of alpha 5 (IV) collagen and assignment of gene to region of the X chromosome containing Alport syndrome locus. Am J Hum Genet. 1990;46:1024–1033.

    PubMed  CAS  Google Scholar 

  28. Basti S, Rathi V, Reddy MK, Gupta S. Clear lens extraction for anterior lenticonus. J Cataract Refract Surg. 1995;21:363–364.

    PubMed  CAS  Google Scholar 

  29. Cheong HI, Kashtan CE, Kim Y, Kleppel MM, Michael AF. Immunohistologic studies of type IV collagen in anterior lens capsules of patients with Alport syndrome. Lab Invest. 1994;70:553–557.

    PubMed  CAS  Google Scholar 

  30. Grondalski SJ, Bennett GR. Alport's syndrome: review and case report. Optom Vis Sci. 1989;66:396–398.

    Article  PubMed  CAS  Google Scholar 

  31. McCartney PJ, McGuinness R. Alport's syndrome and the eye. Aust NZ J Ophthalmol. 1989;17:165–168.

    CAS  Google Scholar 

  32. Streeten BW, Robinson MR, Wallace R, Jones DB. Lens capsule abnormalities in Alport's syndrome. Arch Ophthalmol. 1987;105:1693–1697.

    PubMed  CAS  Google Scholar 

  33. Brazier DJ, Neild GH. Eye problems in a family with Alport's syndrome. Nephrol Dial Transplant. 1996;11:2351–2352.

    PubMed  CAS  Google Scholar 

  34. Atkin CJ, Hasstedt SJ, Menlove L, et al. Mapping of Alport syndrome to long arm of X chromosome. Am J Hum Genet. 1988;42:249–255.

    PubMed  CAS  Google Scholar 

  35. Vanderschueren A, Stalmans I, Lombaerts R, Leys A. Ocular abnormalities in patients with Alport's syndrome. Nephrol Dial Transplant. 1996;11:2355–2358.

    PubMed  CAS  Google Scholar 

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Sathish, K.R., Chandrashekar, Pai, V. et al. Spontaeous capsular ruptures in alport syndrome. Ann Ophthalmol 33, 131–135 (2001). https://doi.org/10.1007/s12009-001-0008-y

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