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Paper Details

From Feeding Challenges to Oral-Motor Dyspraxia: A Comprehensive Description of 10 New Cases with CTNNB1 Syndrome.
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2023
CTNNB1, CTNNB1 Syndrome, Children, Oral-Motor Dyspraxia, Sialorrhea, autosomal-dominant neurodevelopmental disorder, coordination difficulties, developmental delay, drooling, facial features, gene variants, intellectual disability, movement disorders, oral-motor dyspraxia, patients, visual defects
Author NameAffiliation
Maria Cristina DigilioIRCCS Bambino Gesu Children Hospital
Marco TartagliaIRCCS Bambino Gesu Children's Hospital
Giuseppe ZampinoCenter for Rare Diseases and Birth Defects, Fondazione Policlinico Universitario A. Gemelli IRCCS
Giuseppe ZampinoUniversita Cattolica del Sacro Cuore
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Release 1.2