The clinical picture described here—prominent cerebellar involvement within a broader NDD—overlaps with other early‐onset autosomal recessive conditions (Table S3), including CA8, WDR81, ATP8A2, GPAA1, and VLDLR‐related disorders.25, 26, 27, 28, 29, 30, 31, 32, 33. This evidence concerns the gene CA8 and Neurodevelopmental delay.