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PGY-2s: OKAPs done!

Discussion in 'Ophthalmology: Eye Physicians & Surgeons' started by rubensan, Apr 14, 2007.

  1. rubensan

    rubensan Senior Member Moderator Emeritus 5+ Year Member

    Jan 27, 2005
    Pasadena, CA
    OKAPs done! 2 and 1/2 months left of first year! discuss!:D
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  3. odieoh

    odieoh Member 10+ Year Member

    Jun 25, 2003
    Well, glad thats over with. Anyone know what that mystery instrument was on the test?
  4. guttata

    guttata Member 7+ Year Member

    Nov 19, 2003
    Did -anyone- think it was harder this year compared the last year? I may be in trouble....
  5. eyerish


    Jan 17, 2007
    The PGY-3's in my program said the same, if that helps. :thumbup:
  6. Visionary

    Visionary Medical Retinologist Physician 10+ Year Member

    Dec 19, 2003
    So you think that was pigmented paravenous, too? One of my fellow residents thinks it was DUSN, and that's why they showed the other (normal) fundus shot. There did seem to be definite pigmentation only around the venules, though.

    BTW, are we breaking any rules by discussing OKAP topics on this forum?
  7. rubensan

    rubensan Senior Member Moderator Emeritus 5+ Year Member

    Jan 27, 2005
    Pasadena, CA
    i think it is a violation to reproduce the test in any way. the above posts have been unapproved...whatever that means. please delete any post that contains test content in any way. the original purpose of the thread was to discuss the relief after taking the OKAPs rather than the actual questions. sorry....

  8. NDeyeMD

    NDeyeMD New Member

    Oct 25, 2005
    I thought it was DUSN, since the nerve was pale, and it was unilateral. It also did not look like the PPRA on last year's test. The classic Description of PPRA is bilateral.

    Here's an excerpt from a case report in Nature:

    Pigmented paravenous retinochoroidal atrophy (PPRA) is an uncommon disease characterised by paravenous zones of retinal degeneration with bone spicule pigmentation.1,2,3,4,5,6,7,8,9 This is an asymptomatic disease usually detected during routine ophthalmic examination. The condition is generally bilateral and young adults are most commonly affected. The cause of the disease is unknown although an inflammatory10 or hereditary11 aetiology has been suggested. We report a case with typical fundus appearance of paravenous pigmented retinochoroidal atrophy accompanied by an active inflammation with cystoid macular edema.

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