A Rare Missense Variant in TNPO2 in an Individual With a Neurodevelopmental Disability.

Ryan Cohen1, Mythily Ganapathi2, Alban Ziegler1

  • 1Department of Pediatrics, Columbia University Irving Medical Center, New York, New York, USA.

Summary

A novel variant in the Transportin-2 (TNPO2) gene was identified in an elderly patient with a history of intellectual disability and cognitive decline. This finding suggests TNPO2 variants may cause intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies (IDDHISD).

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