Title of article
Location, ubtructure, and compoition of baal laminar druen compared with druen aociated with aging and age-related macular degeneration
Author/Authors
tephen R. Ruell، نويسنده , , Robert F. Mullin، نويسنده , , Bobbie L. chneider، نويسنده , , Gregory . Hageman، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2000
Pages
10
From page
205
To page
214
Abstract
PURPOE:
To determine whether baal laminar druen differ in their location, ultratructure, or compoition from druen aociated with aging and age-related macular degeneration.
METHOD:
A paraffin-embedded block from an eye of a patient with baal laminar druen wa obtained. ection were examined immunohitochemically uing a battery of antibodie and lectin directed againt druen-aociated protein and glycoconjugate, repectively. Thin ection were examined by electron microcopy and compared with eye with age-related macular degeneration.
REULT:
Druen in the eye with baal laminar druen are located between the baal lamina of the retinal pigment epithelium and the inner collagenou layer of Bruch membrane, jut a they are in age-related macular degeneration. Two ditinct ultratructural phenotype are oberved in the eye with baal laminar druen; their ubtructure i inditinguihable from druen phenotype in age-related macular degeneration. Both baal laminar druen and druen aociated with age-related macular degeneration are bound by the lectin Ricini communi agglutinin and Arachi hypogea agglutinin (after neuraminidae digetion) and by antivitronectin, anti–HLA-DR, anti–erum amyloid P, and anti-C5 antibodie, but not by antibodie directed againt baement membrane–aociated heparan ulfate proteoglycan, laminin, fibrinogen, or collagen type IV.
CONCLUION:
Thee data upport the notion that cuticular or baal laminar druen are imilar to, and perhap inditinguihable from, druen aociated with age-related macular degeneration and are not nodular or diffue thickening of Bruch membrane, a previouly uggeted. Thu, we ugget baal laminar druen i a minomer. Thi clinical phenotype hould be identified a “early adult onet, grouped druen” or by the eponym “Ga yndrome.” Feature of baal laminar druen, uch a uniform druen ize, clutered ditribution, and angiographic feature, do not appear to be related to difference in druen location, compoition, or ubtructure.
Journal title
American Journal of Ophthalmology
Serial Year
2000
Journal title
American Journal of Ophthalmology
Record number
622683
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