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A Simple Mechanical Procedure to Create Limbal Stem Cell Deficiency in Mouse
Published on: November 17, 2016
Novel corneal features in two males with incontinentia pigmenti
E J Mayer1, G N Shuttleworth, K L Greenhalgh
1Bristol Eye Hospital, Lower Maudlin Street, Bristol BS1 2LX, UK. ericjmayer@hotmail.com
The British Journal of Ophthalmology
|April 26, 2003
Abstract:
Incontinentia pigmenti (IP) is a rare X linked genetic disorder, which predominantly affects females. The mutations are usually lethal in males. Two male cases are presented; a genetic mosaic for the common IP deletion and another in whom the genetic abnormality has not yet been characterised. Emphasis is placed on the ocular features present in this disorder and in particular a novel corneal feature and its possible aetiology.
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