Ocular involvement of Crouzon Syndrome: A Case Report
Journal Title: Scholars Journal of Medical Case Reports - Year 2015, Vol 3, Issue 12
Abstract
Crouzon syndrome is a rare genetic disorder characterized by distinctive malformations of the skull and facial region. Though Crouzon syndrome is inherited as autosomal dominant disorder, many of them are sporadic. We report a case with ocular involvement in A-9-year old female.
Authors and Affiliations
Théra JP, Hughes D, Tinley C, Bamani S, Traoré L
Keywords
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- EP ID EP377768
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