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Scholars Journal of Medical Case Reports | Volume-3 | Issue-12
Ocular involvement of Crouzon Syndrome: A Case Report
Théra JP, Hughes D, Tinley C, Bamani S, Traoré L, Traoré J
Published: Dec. 31, 2015 | 156 136
DOI: 10.36347/sjmcr.2015.v03i12.024
Pages: 1218-1219
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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.