Matches in SemOpenAlex for { <https://semopenalex.org/work/W2632473769> ?p ?o ?g. }
- W2632473769 endingPage "85" @default.
- W2632473769 startingPage "69" @default.
- W2632473769 abstract "Anterior segment development involves important contributions from neural crest cells as well as surface ectoderm. Transcription factors and other genetic influences orchestrate proper morphogenesis. Several forms of anterior segment dysgenesis, such as sclerocornea and Peters anomaly, lead to corneal opacity. However, this traditional terminology allows neither genotype–phenotype correlations nor prediction of outcomes following surgical intervention. A descriptive classification is presented as more valuable alternative. Corneal dystrophies, epibulbar choristomas, peripheral sclerocornea, and CYP1B1 cytopathy are discussed as forms of primary neonatal corneal opacification. Secondary corneal opacification can be congenital, due to kerato-irido-lenticular or irido-trabecular dysgenesis, or acquired following infection, trauma, or metabolic disease. Peters anomaly, aniridia, and Axenfeld-Rieger syndrome are discussed separately. Finally, congenital anomalies of corneal size—microcornea and megalocornea—and shape—cornea plana and keratoglobus—are reviewed." @default.
- W2632473769 created "2017-06-30" @default.
- W2632473769 creator A5039449677 @default.
- W2632473769 creator A5062658387 @default.
- W2632473769 date "2017-01-01" @default.
- W2632473769 modified "2023-10-16" @default.
- W2632473769 title "Corneal Diseases in Children: Congenital Anomalies" @default.
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- W2632473769 doi "https://doi.org/10.1007/978-3-319-55298-9_6" @default.