Epilepsy and white matter abnormality have been reported in DYRK1A-related intellectual disability syndrome; however, the clinical course has yet to be elucidated. Here, we report the clinical course of an 18-year-old male with a novel heterozygous DYRK1A variant (NM_001396.4: c.957C>G, p.Tyr319*); based on previous reports, epilepsy with this syndrome tends to be well controlled. Follow-up MRIs of the patient’s lesion revealed slightly reduced signal intensity compared to the first image.
CITATION STYLE
Okazaki, T., Yamada, H., Matsuura, K., Kasagi, N., Miyake, N., Matsumoto, N., … Maegaki, Y. (2021). Clinical course of epilepsy and white matter abnormality linked to a novel DYRK1A variant. Human Genome Variation, 8(1). https://doi.org/10.1038/s41439-021-00157-7
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