Epilepsy is a serious neurological disorder characterized by abnormal, recurrent, and
synchronous discharges in the brain. Long-term recurrent seizure attacks can cause serious …

CDKL5 deficiency disorder (CDD) is an X-linked brain disorder of young children and is
caused by pathogenic variants in the cyclin-dependent kinase-like 5 (CDKL5) gene …

CDKL5 deficiency disorder (CDD), a rare and severe neurodevelopmental disease caused
by mutations in the X-linked CDKL 5 gene, is characterized by early-onset epilepsy …

Background CDKL5 deficiency disorder (CDD), a severe neurodevelopmental disorder
characterized by early onset epilepsy, intellectual disability, and autistic features, is caused …

Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a rare
neurodevelopmental disease caused by mutations in the X-linked CDKL5 gene. CDD is …

Ataxia–Telangiectasia Mutated (ATM) is a serine/threonine protein kinase principally known
to orchestrate DNA repair processes upon DNA double-strand breaks (DSBs). Mutations in …

The hippocampus is one of the brain areas affected by autism spectrum disorder (ASD).
Individuals with ASD typically have impairments in hippocampus-dependent learning …

Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene cause a rare
neurodevelopmental disorder characterized by early-onset seizures and severe cognitive …

CDKL5 deficiency disorder is a rare genetic disease caused by mutations in the CDKL5
gene. Central apneas during wakefulness have been reported in patients with CDKL5 …

Mutations in the CDKL5 gene are the cause of CDKL5 deficiency disorder (CDD), a rare and
severe neurodevelopmental condition characterized by early-onset epilepsy, motor …