Clinical Features of Optic Disc Drusen in an Ophthalmic Genetics Cohort

<table class="table-group" id="tab1"><tr><td><table class="table"><tr><td class="thead-hr" colspan="2"><hr/></td></tr><tr class="thead"><td class="align_left">Diagnosis</td><td class="align_center">Number of ODD patients (%)</td></tr><tr><td class="thead-hr" colspan="2"><hr/></td></tr><tr><td class="align_left">Retinal degeneration</td><td class="align_center">42 (75)</td></tr><tr><td class="align_left"> Rod-cone dystrophy</td><td class="align_center">36 (64)</td></tr><tr><td class="align_left"> Macular and/or cone-predominant dystrophy</td><td class="align_center">6 (11)</td></tr><tr><td class="align_left">Genetic condition without a retinal degeneration</td><td class="align_center">14 (25)</td></tr><tr><td class="align_left" colspan="2"><hr/></td></tr><tr><td class="align_left">Isolated ocular condition</td><td class="align_center">28 (50)</td></tr><tr><td class="align_left">Syndromic ocular condition</td><td class="align_center">21 (38)</td></tr><tr><td class="align_left">Genetic conditions for which ophthalmic evaluations were requested</td><td class="align_center">7 (12)</td></tr><tr class="table-tr"><td colspan="2"><hr class="tbody-hr"/></td></tr></table></td></tr></table>

Journal of Ophthalmology

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Table 1

Table 1: Clinical Features of Optic Disc Drusen in an Ophthalmic Genetics Cohort 