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Ectrodactyly-ectodermal dysplasia-clefting syndrome causing blindness in a child
Jamie B Rosenberg1, Salim Butrus, Marlet G Bazemore
1Department of Ophthalmology, Montefiore Medical Center, Bronx, New York 10467, USA. Jamiebella78@gmail.com
Abstract:
Ectrodactyly-ectodermal dysplasia-clefting syndrome, the result of a mutation in the gene encoding tumor protein p63, causes ocular surface disease. It is typically progressive, with vision loss in adulthood. We present a case of severe corneal disease, glaucoma, and blindness related to ectrodactyly-ectodermal dysplasia-clefting syndrome in a 3-year-old female patient.
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