Ata
Ataxia | |
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Synonyms | N/A |
Pronounce | N/A |
Specialty | N/A |
Symptoms | Lack of voluntary coordination of muscle movements |
Complications | Falls, difficulty with fine motor tasks |
Onset | |
Duration | |
Types | N/A |
Causes | Genetic, acquired |
Risks | Family history, certain diseases |
Diagnosis | Clinical evaluation, genetic testing, imaging |
Differential diagnosis | N/A |
Prevention | N/A |
Treatment | Physical therapy, occupational therapy, medication |
Medication | N/A |
Prognosis | Varies depending on cause |
Frequency | |
Deaths | N/A |
Ataxia is a neurological sign consisting of lack of voluntary coordination of muscle movements that includes gait abnormality. Ataxia is a non-specific clinical manifestation implying dysfunction of the parts of the nervous system that coordinate movement, such as the cerebellum.
Classification[edit | edit source]
Ataxia can be classified based on the underlying cause or the specific part of the nervous system affected.
Cerebellar Ataxia[edit | edit source]
Cerebellar ataxia is caused by dysfunction of the cerebellum, the part of the brain that is responsible for coordinating voluntary movements. This type of ataxia can result from a variety of causes, including genetic disorders, stroke, tumor, or multiple sclerosis.
Sensory Ataxia[edit | edit source]
Sensory ataxia is caused by loss of proprioception, the sense of the relative position of one's own parts of the body. This can occur due to damage to the dorsal columns of the spinal cord or peripheral nerves, as seen in conditions like tabes dorsalis or peripheral neuropathy.
Vestibular Ataxia[edit | edit source]
Vestibular ataxia is due to dysfunction of the vestibular system, which helps control balance and eye movements. This can be caused by inner ear disorders, such as labyrinthitis or Meniere's disease.
Causes[edit | edit source]
Ataxia can be caused by a variety of factors, which can be broadly categorized into genetic and acquired causes.
Genetic Causes[edit | edit source]
Genetic ataxias are often inherited and can be caused by mutations in specific genes. Examples include:
Acquired Causes[edit | edit source]
Acquired ataxias can result from:
Symptoms[edit | edit source]
The primary symptom of ataxia is a lack of coordination, which can affect various parts of the body. Symptoms may include:
- Unsteady gait
- Poor coordination of hands, arms, and legs
- Difficulty with fine motor tasks, such as writing or buttoning a shirt
- Slurred speech
- Nystagmus (involuntary eye movements)
Diagnosis[edit | edit source]
Diagnosis of ataxia involves a thorough clinical evaluation, including a detailed medical history and physical examination. Additional tests may include:
- Magnetic resonance imaging (MRI) to look for structural abnormalities in the brain
- Genetic testing to identify hereditary ataxias
- Blood tests to check for metabolic or nutritional causes
Treatment[edit | edit source]
Treatment of ataxia depends on the underlying cause. While there is no cure for many forms of ataxia, supportive therapies can help manage symptoms. These may include:
- Physical therapy to improve balance and coordination
- Occupational therapy to assist with daily activities
- Medications to treat specific symptoms, such as tremors or spasticity
Prognosis[edit | edit source]
The prognosis for individuals with ataxia varies widely depending on the cause and severity of the condition. Some forms of ataxia may progress slowly, while others may lead to significant disability.
See also[edit | edit source]
Classification |
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External resources |
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Contributors: Prab R. Tumpati, MD