Author: Chandra Aman Aragon-Martin Jose Antonio
Publisher: Informa Healthcare
ISSN: 1381-6810
Source: Ophthalmic Genetics, Vol.34, Iss.1-2, 2013-06, pp. : 78-82
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Abstract
Craniosynostosis with ectopia lentis has been described five times since 1950 with unknown inheritance and variable phenotype. The patient was diagnosed with right coronal synostosis at age 10 weeks requiring surgery, and bilateral ectopia lentis with high myopia at 10 months. No other family member was affected. There is no known consanguinity within the family. Genetic screening ruled out
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