Lens development and disorders - clinical diagnosis and treatment

Published on May 31, 2016   31 min
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This is the second lecture dealing with lens development and lens development disorders. My name is Professor Chris Lloyd. I'm a consultant ophthalmologist at Great Ormond Street Hospital in London. I'm also an honorary consultant at Manchester Royal Eye hospital and honorary professor of pediatric ophthalmology at Manchester Academic Health Sciences Center in the University of Manchester.
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Congenital aphakia is an extremely rare malformation of the eye. It's usually associated with other ocular malformations. It can be caused by rubella syndrome or other early teratogenic influences during the first four weeks of gestation. It can be caused by homozygous mutations in the FOXE3 gene, as illustrated by the graphic to the right. This is a case that was published in Molecular Vision six years ago. It can also occur as a secondary phenomenon due to persistent fetal vasculature.
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Microspherophakia is a clinical description of a spherical lens, a lens that is reduced in its natural dimensions. This can be caused by several conditions. These include mutations in the LTB2 gene, Weill-Marchesani syndrome, homocystinuria, and other pan-ocular disorders, like Aniridia or Axenfeld-Rieger syndrome, which cause damage to the zonule.
1:31
Lens duplication is also extremely rare. It's associated with corneal metaplasia, uveal coloboma, and cornea plana, or flattening of the cornea. It's presumed to be due to abnormal lens placode formation. The case illustrating this is published in the Indian Journal of Ophthalmology.
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Lens development and disorders - clinical diagnosis and treatment

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