Abstract
Colobomas of the choroid are a subset of uveal colobomas which result from disruption of the normal process of ocular development during organogenesis. This disruption causes a thinning or absence of a portion of the choroid. Choroidal colobomas may be isolated, associated with other ocular features such as microphthalmos, or associated with systemic features such as papillorenal syndrome and CHARGE syndrome.
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Carey, A., Arevalo, J.F. (2019). Coloboma of the Choroid. In: Ohji, M. (eds) Surgical Retina. Retina Atlas. Springer, Singapore. https://doi.org/10.1007/978-981-13-6214-9_8
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DOI: https://doi.org/10.1007/978-981-13-6214-9_8
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