Ophthalmic manifestations in neurofibromatosis type 1

作者: Michael Kinori , Nickisa Hodgson , Janice Lasky Zeid

DOI: 10.1016/J.SURVOPHTHAL.2017.10.007

关键词: DermatologyPathologyDiseaseInherited diseaseGenetic testingClinical diagnosisNeurofibromatosisMedicine

摘要: Neurofibromatosis type 1 (NF1) is a relatively common multisystemic inherited disease and has been extensively studied by multiple disciplines. Although genetic testing confirmation are available, NF1 remains clinical diagnosis. Many manifestations of involve the eye orbit, ophthalmologist, therefore, plays significant role in diagnosis treatment patients. Improvements diagnostic imaging instruments have provided new insight to study ophthalmic disease. We provide comprehensive up-to-date overview ocular orbital NF1.

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