Ataxia Is a Type of Health Issue Which Makes the Individual Loose the Control of Muscles

 

Ataxia

Ataxia is a neurological disorder that can affect both children and adults. In children, the symptoms are often similar to those of other neurological disorders, but in adults, it can be more severe. Several tests can help the physician finds the cause of the symptoms, including blood tests, MRIs, and other imaging tests. The first step in treating ataxia is to determine whether it is a cause of another condition.

The first step is a neurological examination. The doctor will perform a CT scan and MRI to examine the brain's structure. Other tests include spinal fluid tests, which involve drawing spinal fluid and sending it to a lab for testing. Genetic testing is also recommended to rule out genetic forms of ataxia. Treatment for ataxia will depend on the type of ataxia type. Since there is no single treatment for ataxia, there is no set treatment for it. Acquired Ataxia can be treated with medication or through surgery. It can be treated with exercises. There are various forms of the condition. Friedreich ataxia is the most common type. Affected individuals have a faulty gene in one or both sides of their genomes. It can be inherited from both parents, making it a hereditary condition. However, if the underlying cause is not found, it may be curable with medication.

The cause of ataxia will determine the treatment. The diagnosis of sporadic ataxia can be based on a family history of the disease. In rare cases, patients may be diagnosed with episodic ataxia and a specific gene mutation, such as POLG. A full diagnostic workup can help determine if there is a genetic disorder that causes ataxia. It is vital to note that there is currently no known cure for ataxia.

Ataxia is caused by a malfunction in the cerebellum. This disorder is hereditary. A child receives two copies of every gene from his or her parents. The mutated gene in a person with ataxia is the main cause of the disorder. There is no known cure for ataxia, but treatment will depend on the cause. This disease affects the body's ability to use sensory inputs.

A family history of ataxia can be hereditary. The symptoms of hereditary ataxia may occur at birth or in adulthood. The severity of the condition depends on the type of ataxia and the type of mutation. For sporadic ataxia, the symptoms usually appear in adulthood and do not have a family history. The symptoms of ataxia may range from slurred speech to difficulty walking to severe cognitive impairment.

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If the symptoms of ataxia are more severe, they can affect breathing. In severe cases, these symptoms can be fatal. Special care is necessary for the person with ataxia to avoid complications. Adaptive devices can help the patient manage the disease and maintain a normal life. Moreover, medicines can be prescribed to relieve symptoms. Research is ongoing to find the exact cause of ataxia and find a cure for it. The symptoms of ataxia are difficult to control.

If the symptoms are a sign of ataxia, a doctor should examine the patient carefully. Ataxia is often associated with several associated symptoms, including impaired consciousness, trouble speaking, or swallowing. Other symptoms associated with ataxia include focal sensory loss, vertigo, a slow and abnormal gait, and cognitive impairment. A doctor will also look for any physical changes that may be related to the disorder.

The most common symptoms of ataxia are a lack of balance and coordination. Adaptive devices can help people with ataxia move around with a cane, crutches, or a wheelchair. A healthcare provider will take a complete medical history and perform a physical examination. Symptoms of ataxia can include a loss of sensation in the feet. The person may have difficulty with walking, standing, or balancing.