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Unilateral Peters' anomaly in a patient with DiGeorge syndrome
1Department of Ophthalmology, University Hospitals Leuven, Leuven, Belgium.
Journal of Pediatric Ophthalmology and Strabismus
|October 28, 2005
Abstract:
We report a case of unilateral Peters' anomaly in a 3-month-old infant with a microdeletion in chromosome 22q11.2, a finding not previously described. This anterior segment anomaly can be explained by a problem in neural crest development, as neural crest cells are known to play a role in the developmental defects of this disorder.
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The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
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