Management Team

Dystonia

Overview

Dystonia is a neuromuscular condition characterised by abnormal posturing and turning or twisting movements of the head, trunk, or limbs.

  • Based on the affected body part
    • Generalized dystonia (affects all or most body parts)
    • Focal dystonia (affects one body part)- blepharospasm, cervical dystonia, oromandibular dystonia, truncal dystonia, and writer’s cramp
    • Multifocal dystonia (affects ≥2 unrelated body parts)
    • Segmental dystonia (affects ≥2 adjacent body parts)
    • Adult-onset dystonia is generally focal, whereas those beginning in childhood may become generalized.
  • Based on the cause
    • Inherited- caused due to gene mutation
    • Acquired- secondary to drug, brain injury, stroke, infection, metabolic
    • Idiopathic- no clear cause
  • Based on the symptoms
    • Dopa- responsive dystonia improves dramatically with dopamine supplementation
    • Myoclonus dystonia
    • Paroxysmal dystonia
    • Tardive dystonia
    • Functional dystonia

People with dystonia may experience:

  • Muscle spasms or cramps
  • Postural deformities
  • Difficulty in speaking, chewing, swallowing, walking, and writing
  • Abnormal eye blinking/ contraction of face
  • Bending or twisting of the body

The exact cause is unknown, but may be linked to:

  • Dysfunction of basal ganglia (a brain region controlling movement)
  • Genetic factors
  • Brain injuries
  • Infections or metabolic conditions

Doctors use the following to confirm diagnosis and rule out other causes:

  • Clinical evaluation: observing posture and movements
  • Genetic testing: to identify inherited dystonia
  • MRI Brain and PET scan: for acquired and degenerative causes

Although there is no complete cure, treatments can reduce symptoms and improve quality of life:

  • Medications (anticholinergics, dopamine blockers)
  • Botulinum toxin injections for focal dystonia
  • Physical therapy and rehabilitation to improve muscle control
  • Surgery (deep brain stimulation) for severe cases not responding to medicines
  • Lifestyle modification (stress management, regular exercises)

Seek medical attention if you notice:

  • Persistent involuntary twisting or abnormal posture
  • Difficulty with speech, writing, chewing, or walking

Dystonia cannot always be prevented, but risk can be reduced by:

  • Avoiding long-term use of certain medications without medical supervision
  • Managing risk factors like stroke, infections, and head injuries

For diagnosis and management of dystonia, consult a Neurologist (specialist in brain and nerve disorders).

Disclaimer:

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