CDKL5 deficiency disorder

CDKL5 deficiency disorder
Synonyms	CDKL5 disorder, X-linked infantile spasm syndrome 2
Pronounce	N/A
Specialty	N/A
Symptoms	Seizures, developmental delay, intellectual disability, motor dysfunction, vision impairment
Complications	N/A
Onset	Infancy
Duration	Lifelong
Types	N/A
Causes	Genetic mutation in the CDKL5 gene
Risks	Family history of the disorder
Diagnosis	Genetic testing, clinical evaluation
Differential diagnosis	Rett syndrome, West syndrome, Lennox-Gastaut syndrome
Prevention	N/A
Treatment	Antiepileptic drugs, physical therapy, occupational therapy, speech therapy
Medication	N/A
Prognosis	Varies, often involves significant disability
Frequency	Estimated 1 in 40,000 to 60,000 live births
Deaths	N/A

CDKL5 deficiency disorder (CDD) is a rare neurological disorder that primarily affects females and is characterized by early-onset epileptic seizures, severe intellectual disability, and motor impairment. The disorder is caused by mutations in the CDKL5 gene, which is involved in brain development.

Etiology

CDD is caused by mutations in the CDKL5 gene, which provides instructions for making a protein that is essential for normal brain development. This protein acts as a kinase, which is a type of enzyme that modifies other proteins by adding a phosphate group (a process called phosphorylation). The CDKL5 protein is thought to play a key role in regulating the connections between neurons (synapses) and the formation of dendritic spines, which are small outgrowths from neurons that help transmit signals from one neuron to another.

Clinical Presentation

The most common symptoms of CDD include early-onset epileptic seizures, severe intellectual disability, and motor impairment. Seizures typically begin in the first few months of life and can be resistant to treatment. Intellectual disability is severe and most individuals with CDD are unable to speak. Motor impairment is also severe, with many individuals unable to walk or control their movements.

Diagnosis

Diagnosis of CDD is based on clinical symptoms and confirmed by genetic testing to identify mutations in the CDKL5 gene. Because the symptoms of CDD can be similar to other neurological disorders, it is often misdiagnosed as Rett syndrome or infantile spasms.

Treatment

There is currently no cure for CDD, and treatment is focused on managing symptoms. This can include medications to control seizures, physical and occupational therapy to improve motor skills, and special education services to address intellectual disability.

Research

Research into CDD is ongoing, with scientists working to better understand the function of the CDKL5 protein and how mutations in the CDKL5 gene lead to the symptoms of the disorder. This research could potentially lead to new treatments for CDD in the future.

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