HIGHLIGHTS
- What: The authors aimed to contrast the neurodevelopmental and behavioural phenotype of children with SYNGAP1-related ID (SYNGAP1-ID) to children with other monogenic conditions and a matched degree of ID. For the first time the authors demonstrate that SYNGAP1-ID is associated with fine motor and language difficulties beyond those experienced by children with other genetic causes of DD and ID. By comparing SYNGAP1-ID to a heterogenous group of monogenic conditions all associated with ID the authors aimed to mimic this clinical challenge and further aid clinicians in identifying SYNGAP1-associated features and providing appropriate . . .

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