Abstract | BACKGROUND: CONCLUSION: Case 1 was a typical SLS, and case 2 was a rare one with fundus lesions simulating Coats disease, keratoconus, and cataract. We suspect the exudative changes resulted from various vessel changes and choroidal circulatory disturbance of renal retinopathy, retinal vascular damage, and destruction of blood-retinal barrier with retinitis pigmentosa, the inflammatory changes of vessels, and other things.
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Authors | Tokuhide Oyama, Tomoaki Usui, Hiruma Hasebe, Atsushi Miki, Shigeaki Matsumoto, Kieko Suda, Nobuko Saito, Kazuyuki Imai, Mineo Takagi, Toyohisa Yoshizawa, Haruki Abe |
Journal | Nippon Ganka Gakkai zasshi
(Nippon Ganka Gakkai Zasshi)
Vol. 108
Issue 1
Pg. 29-37
(Jan 2004)
ISSN: 0029-0203 [Print] Japan |
PMID | 14969091
(Publication Type: Case Reports, English Abstract, Journal Article)
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Topics |
- Adolescent
- Electroretinography
- Fundus Oculi
- Humans
- Keratoconus
(complications)
- Kidney Failure, Chronic
(etiology)
- Male
- Polycystic Kidney, Autosomal Recessive
(complications, genetics)
- Retinitis Pigmentosa
(complications, genetics)
- Syndrome
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