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Wallenberg Syndrome - Symptoms and Treatment - Oren Zarif - Wallenberg Syndrome

Wallenberg syndrome is not completely understood by doctors and is not a disease with a known cure. The disorder may be triggered by a physical or psychological trauma, chronic underlying disease, or an autoimmune condition. In many cases, however, doctors have found that treatment is dependent on the individual's symptoms and medical history. Listed below are some symptoms and treatment options. In some cases, though, medications may be prescribed to treat the disorder.

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The prognosis of Wallenberg syndrome depends on the severity of damage and the location of the stroke in the brainstem. Some people with less damage can recover fully in a matter of weeks to months. Those who suffer from more extensive damage may face a longer recovery period and even permanent disabilities. For these reasons, it is vital to discuss your long-term outlook with your doctor and follow his treatment plan closely. This way, you can maximize your chances of having a successful outcome.

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As a result of the stroke, the blood supply to the brain stem is interrupted. As a result, a group of symptoms, including difficulty swallowing, dizziness, hoarseness, nausea, and nystagmus, will occur. Treatment for Wallenberg syndrome is usually focused on speech therapy and medication. Early treatment can significantly reduce the risk of long-term neurological damage. You should seek medical help if you notice any of these symptoms. The treatment for Wallenberg syndrome will depend on the severity and duration of the symptoms.

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A treatment plan for Wallenberg syndrome will depend on how severe the stroke was and the severity of the associated symptoms. Although most patients recover well, many will have persistent problems with balance and walking. Physical and occupational therapy are vital for the recovery process. While it may not be permanent, it can improve your quality of life. If you are diagnosed with Wallenberg syndrome, your doctor will determine if your treatment should include medications to reduce your risk of another stroke.

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The most common causes of Wallenberg syndrome include arterial dissection, cardiac embolism, or vertebral artery disease. Symptoms may also occur if an artery is occluded. Regardless of the cause, you should seek medical attention if you suspect that you may be suffering from the syndrome. While the prognosis is generally good, it is best to have an MRI to confirm if you have the condition.

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Symptoms of the syndrome may include hiccups, diplopia, and unilateral posterior headache. In some cases, patients with lateral medullary syndrome may also experience unidirectional nystagmus and mild imbalance. Several patients may exhibit dysphagia, a common symptom of Wallenberg syndrome. However, this symptom may be transient and return in a matter of months. The patient should undergo further evaluation if symptoms persist for more than two weeks.

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A physician can also develop a neurovascular disease that causes symptoms similar to the symptoms of Wallenberg syndrome. In 1894, Wallenberg performed a post-mortem on a patient who suffered from this condition. His post-mortem confirmed the presence of a lesion in the posterior inferior cerebellar artery. As a result, Wallenberg symptomatic treatment became available in the late 19th century. A few cases have been reported since then.

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LMI is a primary cause of dysphagia in Wallenberg syndrome. The neuronal damage in the nucleus ambiguus disrupts the link between the two swallowing centers, the NA and NTS. The remaining premotor neurons may be the cause of dysphagia in WS, although the contralateral center of the medulla oblongata can compensate for the loss of these neurons. Therefore, a thorough understanding of the neurological changes that cause this disease will be required to develop a treatment plan for this condition.

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Swallowing disorders associated with WS are common in patients who have hemispheric stroke. The symptoms are usually more prominent than those of patients without stroke. The laryngeal elevation is delayed in patients with WS compared with normal individuals, and patients with unilateral involvement of the 9th and 10th cranial nerves have a greater risk for dysphagia. Patients with WS also have difficulties controlling the bolus during swallowing.

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Because of the widespread nature of the syndrome, it can be difficult to diagnose. A physician with this condition must have received specialized training to diagnose and treat the disease. There are many ways to learn more about the condition. You can also seek assistance from the National Institutes of Health's Genetic and Rare Diseases Information Center. These resources may also be helpful in finding a treatment for wallenberg syndrome. This condition may not be easily treatable, but it can still be treated.

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