Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development (Molecular Psychiatry, (2023), 28, 4, (1647-1663), 10.1038/s41380-022-01764-8)

Abstract

Wording was altered for the discussion. Only two probands (11%) with genetic diagnoses (SETD1B (ID10), ERF (ID18)) had CAS without co-occurring neurodevelopmental disorder diagnoses. One was aged 10;8 years, had average IQ and was attending a school for children with specific speech and language impairment. The other child was only 4;7 years and had not yet had IQ testing because no concerns had been raised by his treating physician, family or preschool teacher regarding his general learning ability; however, it is possible that other neurodevelopmental diagnoses could still be made into the future. These findings expand the spectrum of phenotypes associated with these conditions. SETD1B has..