Glaucoma and degenerative vitreoretinopathy in a girl with Nicolaides-Baraitser syndrome

We report the case of a 12-year-old girl diagnosed with Nicolaides-Baraitser syndrome with novel ocular features. Diagnosis was based on clinical features, including developmental delay, sparse hair, and craniofacial features along with de novo mutation in SMARCA2 . Eye findings included bilateral glaucoma, cataracts, and degenerative vitreoretinopathy. Given the absence of an associated recognizable disorder and the low prevalence of the low prevalence of these ocular findings in the general population, we suggest that these ocular features may not be chance association.