<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tatesi, B. Faculty of Medical Sciences, &quot;Goce Delchev&quot; University, Stip, North Macedonia</style></author><author><style face="normal" font="default" size="100%">Pandilov, S. PHI University Clinic for Eye Diseases - Skopje, Republic of North Macedonia</style></author><author><style face="normal" font="default" size="100%">Mageroska Spirkoska, A. PHI General Hospital with extended activity, Department of Ophthalmology – Prilep, North Macedonia</style></author><author><style face="normal" font="default" size="100%">Pepelasheva Jovanova, E.PHI General Hospital, Department of Ophthalmology – Veles, Republic of North Macedonia</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">BILATERAL UVEAL COLOBOMA IN COMBINATION WITH A SYSTEMIC SYNDROME – A CASE REPORTAuthors</style></title><secondary-title><style face="normal" font="default" size="100%">Academic Medical Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.doi.org/10.53582/AMJ2443127t</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">2024;4</style></volume><pages><style face="normal" font="default" size="100%">127-132</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;p1&quot;&gt;&lt;strong&gt;Abstract&lt;/strong&gt;&lt;/p&gt;
&lt;p class=&quot;p1&quot;&gt;Coloboma of the uvea is a relatively rare ophthalmic entity, which occurs as a result&amp;nbsp;of a disturbance in the process of closing the embryonic optic fissure. It can be hereditary,&amp;nbsp;sporadic or part of systemic syndromes. Each of the structures of the uveal tract, alone or&amp;nbsp;together, unilaterally or bilaterally, can have the presence of a coloboma. In this paper, we&amp;nbsp;describe the case of a 9-year-old girl with bilateral coloboma and accompanying ectrodactyly&amp;nbsp;of the lower limbs, probably as part of a syndrome - Ectrodactyly-ectodermal dysplasia-cleft&amp;nbsp;syndrome. The patient is regularly monitored with biomicroscopic and funduscopic&amp;nbsp;examination supplemented with posterior optical coherence tomography and perimetry, with&amp;nbsp;the aim of timely recognition of possible ophthalmic complications.&lt;/p&gt;
&lt;p class=&quot;p1&quot;&gt;&lt;strong&gt;Keywords:&lt;/strong&gt;&amp;nbsp;coloboma, uvea, ectrodactyly, congenital malformation&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue></record></records></xml>