Ectrodactyly-ectodermal dysplasia-clefting syndrome causing blindness in a child

Jamie B. Rosenberg, Salim Butrus, Marlet G. Bazemore

Research output: Contribution to journalArticlepeer-review

8 Scopus citations


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.

Original languageEnglish (US)
Pages (from-to)80-82
Number of pages3
JournalJournal of AAPOS
Issue number1
StatePublished - Feb 2011

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Ophthalmology


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