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Does Benign Paroxysmal Tonic Upgaze have a cure?

Here you can see if Benign Paroxysmal Tonic Upgaze has a cure or not yet. If there is no cure yet, is Benign Paroxysmal Tonic Upgaze chronic? Will a cure soon be discovered?

Benign Paroxysmal Tonic Upgaze cure

Benign Paroxysmal Tonic Upgaze (BPTU) is a rare neurological disorder characterized by abnormal upward eye movements.


Currently, there is no known cure for BPTU. However, treatment options such as physical therapy, medication, or surgical interventions can help manage the symptoms and improve quality of life for individuals with BPTU.


It is important to consult with a healthcare professional for a proper diagnosis and to discuss the most suitable treatment plan.



Benign Paroxysmal Tonic Upgaze (BPTU) is a rare neurological disorder that primarily affects infants and young children. It is characterized by the involuntary upward deviation of the eyes, often accompanied by a backward head tilt. The exact cause of BPTU is still unknown, and there is currently no known cure for this condition.



Although there is no cure, treatment options are available to manage the symptoms and improve the quality of life for individuals with BPTU. The most common approach is to use prism glasses to correct the abnormal eye position and allow for better vision. These glasses can help alleviate the upward gaze and head tilt, enabling affected individuals to maintain a more natural head position.



In some cases, physical therapy may be recommended to help improve balance and coordination, as well as to address any associated motor delays. This therapy can assist in minimizing the impact of BPTU on a child's development and overall functioning.



It is important for individuals with BPTU to receive regular medical follow-ups to monitor their condition and ensure that any changes or new symptoms are addressed promptly. While the condition itself is considered benign and does not typically worsen over time, ongoing management and support are crucial.



Research is ongoing to better understand the underlying causes of BPTU and to explore potential future treatment options. However, at present, the focus remains on symptom management and maximizing the individual's functional abilities.


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Layla was diagnosed with PTU and episodic Ataxia at the ageof 17months. Now she is almost 4 and each day is a new day with alot of improvements and often new challenges. We are lucky to have such a happy little girl that takes all of her challenges i...

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