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Post Date: June 13, 2022
WHAT IS CDKL5 DEFICIENCY DISORDER?
Published by: International Foundation for CDKL5 Research CDKL5 deficiency disorder is a rare developmental epileptic encephalopathy caused by mutations in the CDKL5 gene, and this can manifest in a broad range of clinical symptoms and severity. The hallmarks are early-onset, intractable epilepsy and neurodevelopmental delay impacting cognitive, motor, speech, and visual function. Although rare, the […]
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