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CTNNB1-related neurodevelopmental disorder and/or vitreoretinopathy

Any neurodevelopmental disorder and/or exudative vitreoretinopathy caused by a monoallelic variant in the CTNNB1 gene. Variants in CTNNB1 are related to a neurodevelopmental condition with a broad spectrum of presentations ranging from isolated vitreoretinopathy to a complex neurodevelopmental disorder with mild to severe intellectual disability, microcephaly, spasticity, autism spectrum disorder, and visual defects, including retinal detachment, and abnormal retinal vascularization.

3 trials tagged with this condition →

Severe intellectual disability-progressive spastic diplegia syndrome 4 trials
Exudative vitreoretinopathy 7 0 trials