Genetic torsion dystonia
ICD-10 G24.1 is a billable code used to indicate a diagnosis of genetic torsion dystonia.
Genetic torsion dystonia is a movement disorder characterized by sustained muscle contractions, abnormal postures, and twisting movements. It is primarily caused by genetic mutations affecting the basal ganglia, which play a crucial role in motor control. Patients often experience involuntary muscle contractions that can lead to significant disability and discomfort. The condition can manifest in various forms, including generalized dystonia, which affects multiple body parts, or focal dystonia, which is limited to a specific area such as the neck or hand. Genetic torsion dystonia is often associated with other neurological conditions, including Parkinson's disease and other extrapyramidal disorders. The onset of symptoms typically occurs in childhood or early adulthood, and the severity can vary widely among individuals. Treatment options may include dopaminergic medications, botulinum toxin injections, and physical therapy, aimed at alleviating symptoms and improving quality of life. Accurate diagnosis and coding are essential for appropriate management and reimbursement, as the condition can overlap with other movement disorders.
Detailed neurological examination findings, genetic testing results, and treatment plans.
Diagnosis of genetic torsion dystonia in a patient with a family history of movement disorders.
Ensure that genetic testing results are included in the medical record to support the diagnosis.
Functional assessments, treatment goals, and response to therapy.
Rehabilitation interventions for a patient with dystonia affecting mobility.
Document the impact of dystonia on daily activities and quality of life.
Used for treating focal dystonia in patients with G24.1.
Document the specific muscles injected and the patient's response to treatment.
Neurology specialists should ensure that the treatment plan aligns with the diagnosis.
Genetic torsion dystonia is primarily caused by mutations in specific genes that affect motor control, particularly those impacting the basal ganglia.
