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Updated: Jul 3, 2025

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Published on: May 12, 2015
Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorder
Khurram Liaqat1, Kayla Treat1, Theodore E Wilson2
1Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA.
Abstract:
A 5-year-old affected male had following phenotypes: autism, motor stereotypy, developmental regression, staring gaze, absent speech, and behavioral abnormality. The biochemical testing was normal and genetic testing identified a de novo pathogenic variant in ITSN1 gene in the proband. To our knowledge, this is the second report that elucidates the role of ITSN1 gene in an autosomal dominant neurodevelopmental disorder.
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