Ocular Disorders and Treatments
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Scope of this subject
This cluster of papers focuses on genetic and clinical studies related to ocular development, particularly microphthalmia, anophthalmia, and associated syndromes such as Fraser syndrome. It explores the genetic mutations in genes like SOX2 and BCOR, as well as the use of orbital implants in surgical management of eye malformations. The research also delves into epidermal adhesion and its role in ocular development.
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Research vocabulary
congenital eye malformation; microphthalmia; eye development; ocular prosthesis; anophthalmia; coloboma; ocular malformations; aniridia; orbital implants; hereditary eye disease; congenital ptosis; lens development; optic nerve hypoplasia; pediatric eye disease; anterior segment dysgenesis; iris coloboma; congenital aniridia; eyelid malformation; orbital prosthesis; persistent hyperplastic primary vitreous; Axenfeld-Rieger syndrome; microcornea; anophthalmic socket; optic disc anomaly; implant exposure
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Numeric address and provenance
Morton address: 38285563971563087 · morton4x16-v1
Coordinates: (1, 13, 1311, 12989). The address interleaves categorical identifier bits. Nearby addresses are not guaranteed to describe semantically similar subjects.
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