Anterior Lens Capsule Abnormalities in Alport Syndrome.
- Author:
Jae Hyuk CHOI
1
;
Kyung Sool NA
;
Seon Hee BAE
;
Gyoung Hwan ROH
Author Information
- Publication Type:Case Report
- Keywords: Alport syndrome; Capsular dehiscence; Lenticonus
- MeSH: Adult; Epithelial Cells/ultrastructure; Humans; Lens Capsule, Crystalline/*ultrastructure; Lens Diseases/genetics/*pathology; Lens Implantation, Intraocular; Male; Nephritis, Hereditary/genetics/*pathology; Phacoemulsification
- From:Korean Journal of Ophthalmology 2005;19(1):84-89
- CountryRepublic of Korea
- Language:English
- Abstract: Alport syndrome is a hereditary, progressive disease characterized by progressive nephritis, sensorineural deafness, and ocular abnormalities, including anterior lenticonus. The ultrastructure of the lens capsule abnormalities in Alport syndrome is reported. Four anterior lens capsules from 31-year-old patient and 26-year-old patient with lenticonus who were affected by the Alport syndrome were obtained at capsulectomy. And all four anterior lens capsules were examined by transmission electron microscopy. The histopathologic findings showed that the thickness of the anterior lens capsules was decreased (4~13 micrometer) and that there were many vascular dehiscences localized at the inner part of the lens capsule. There were large numbers of capsular dehiscences containing fibrillar materials and vacuoles. The anterior capsules were clearly fragile in this disease, forming the basis for the progressive lenticonus and anterior polar cataract.
