Chorea Acanthocytosis

Below you will find more information about Chorea Acanthocytosis from Medigest. If you believe that you are suffering from any of the symptoms of Chorea Acanthocytosis it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Chorea Acanthocytosis and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Chorea Acanthocytosis comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Chorea acanthocytosis is an inherited illness caused by a genetic mutation that disrupts the proteins in red blood cells. When a blood sample is observed under a microscope, some of the red blood cells look thorny, and these are called acanthocytes.


There is no treatment for this disease and eventually leads to death.

Symptoms and Signs

The effects of this disease include behavioral changes, muscle deterioration, epilepsy and neuronal degradation. Symptoms begin to be noticeable when an affected person reaches the age of 35.

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