Truncal ataxia

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Truncal ataxia is a form of ataxia that primarily affects the trunk of the body, causing instability and difficulty in maintaining balance. It is often associated with various neurological disorders, including multiple sclerosis, Friedreich's ataxia, and spinocerebellar ataxia.

Definition[edit | edit source]

Truncal ataxia is characterized by a wide-based gait and difficulty in maintaining balance, especially when sitting or standing. This is due to the inability to coordinate the muscles of the trunk, which are essential for maintaining posture and balance.

Causes[edit | edit source]

Truncal ataxia can be caused by a variety of conditions, most of which are neurological in nature. These include:

  • Multiple sclerosis: This is a chronic disease that affects the central nervous system, causing symptoms such as fatigue, difficulty walking, and truncal ataxia.
  • Friedreich's ataxia: This is a genetic disorder that causes progressive damage to the nervous system, resulting in symptoms such as speech problems, heart disease, and truncal ataxia.
  • Spinocerebellar ataxia: This is a group of hereditary disorders characterized by degenerative changes in the part of the brain related to the control of movement (cerebellum) and sometimes the spinal cord.

Diagnosis[edit | edit source]

The diagnosis of truncal ataxia is typically made based on a combination of clinical examination and medical history. Additional tests, such as MRI, may be used to identify the underlying cause of the ataxia.

Treatment[edit | edit source]

Treatment for truncal ataxia primarily involves managing the underlying condition causing the ataxia. This may involve medication, physical therapy, or in some cases, surgery.

See also[edit | edit source]

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Contributors: Prab R. Tumpati, MD