Developing A NEUROFIBROMATOSIS TYPE 1 OPHTHALMIC screening protocol in a neurofibromatosis type 1 clinic: A single center pilot study

Brief description of study

The purpose of this study is to develop a new way of screening eye diseases in children with NEUROFIBROMATOSIS TYPE 1 (NF1), a genetic condition that may cause eye disease in children. This study will design screening that combines standard of care screening and additional eye imaging at a routine visit at an NF1- specific clinic. Such screening would cut down on the number of visits children with NF1 would need to complete to screen for this condition.


Clinical Study Identifier: s20-02012
Principal Investigator: Zachary Elkin.


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