Infantile convulsions and choreoathetosis

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| Infantile convulsions and choreoathetosis | |
|---|---|
| File:Autosomal dominant - en.svg | |
| Synonyms | N/A |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Seizures, chorea, athetosis |
| Complications | N/A |
| Onset | Infancy |
| Duration | Chronic |
| Types | N/A |
| Causes | Genetic mutation |
| Risks | Family history |
| Diagnosis | Clinical diagnosis, genetic testing |
| Differential diagnosis | Epilepsy, cerebral palsy |
| Prevention | N/A |
| Treatment | Anticonvulsant medications, physical therapy |
| Medication | N/A |
| Prognosis | Variable, often improves with age |
| Frequency | Rare |
| Deaths | N/A |
Infantile convulsions and choreoathetosis is a rare neurological disorder that primarily affects infants and young children. It is characterized by a combination of convulsions (seizures) and choreoathetosis (involuntary, writhing movements).
Symptoms[edit]
Infantile convulsions and choreoathetosis typically presents with episodes of seizures that may involve jerking movements of the arms and legs. These seizures can be accompanied by choreoathetoid movements, which are characterized by continuous, involuntary writhing motions.
Causes[edit]
The exact cause of infantile convulsions and choreoathetosis is not well understood. However, it is believed to have a genetic component, as the disorder tends to run in families. Mutations in certain genes have been associated with the condition.
Diagnosis[edit]
Diagnosis of infantile convulsions and choreoathetosis is based on clinical evaluation, medical history, and genetic testing. Imaging studies such as MRI may be performed to rule out other possible causes of the symptoms.
Treatment[edit]
Treatment for infantile convulsions and choreoathetosis focuses on managing the symptoms and preventing complications. Anticonvulsant medications may be prescribed to control seizures, while physical therapy can help improve motor function.
Prognosis[edit]
The prognosis for individuals with infantile convulsions and choreoathetosis varies depending on the severity of the symptoms and the individual's response to treatment. With appropriate management, many individuals can lead relatively normal lives.
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