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What is ANKRD11 Variants and KBG Syndrome Insights about?

This article discusses the clinical and molecular findings of 23 individuals with variants in the ANKRD11 gene, primarily associated with KBG syndrome and other developmental disorders. The study highlights the overlapping phenotypic features of these disorders, complicating clinical diagnosis, and suggests that ANKRD11 variants may be linked to a broader spectrum of neurodevelopmental syndromes. The findings indicate significant variability in clinical presentation, including developmental delays and dysmo

Author

WMBK MUSIC

Language

EN