@article {5600,
	title = {BILATERAL UVEAL COLOBOMA IN COMBINATION WITH A SYSTEMIC SYNDROME {\textendash} A CASE REPORTAuthors},
	journal = {Academic Medical Journal},
	volume = {2024;4},
	year = {2024},
	pages = {127-132},
	abstract = {Abstract
Coloboma of the uvea is a relatively rare ophthalmic entity, which occurs as a result\&nbsp;of a disturbance in the process of closing the embryonic optic fissure. It can be hereditary,\&nbsp;sporadic or part of systemic syndromes. Each of the structures of the uveal tract, alone or\&nbsp;together, unilaterally or bilaterally, can have the presence of a coloboma. In this paper, we\&nbsp;describe the case of a 9-year-old girl with bilateral coloboma and accompanying ectrodactyly\&nbsp;of the lower limbs, probably as part of a syndrome - Ectrodactyly-ectodermal dysplasia-cleft\&nbsp;syndrome. The patient is regularly monitored with biomicroscopic and funduscopic\&nbsp;examination supplemented with posterior optical coherence tomography and perimetry, with\&nbsp;the aim of timely recognition of possible ophthalmic complications.
Keywords:\&nbsp;coloboma, uvea, ectrodactyly, congenital malformation},
	url = {https://www.doi.org/10.53582/AMJ2443127t},
	author = {Tatesi, B. Faculty of Medical Sciences, "Goce Delchev" University, Stip, North Macedonia and Pandilov, S. PHI University Clinic for Eye Diseases - Skopje, Republic of North Macedonia and Mageroska Spirkoska, A. PHI General Hospital with extended activity, Department of Ophthalmology {\textendash} Prilep, North Macedonia and Pepelasheva Jovanova, E.PHI General Hospital, Department of Ophthalmology {\textendash} Veles, Republic of North Macedonia}
}
