The risk factors for Gerstmann Syndrome may include:
It is important to note that having a risk factor does not mean that one will get the condition. A risk factor increases one’s chances of getting a condition compared to an individual without the risk factors. Some risk factors are more important than others.
Also, not having a risk factor does not mean that an individual will not get the condition. It is always important to discuss the effect of risk factors with your healthcare provider.
The cause of Gerstmann Syndrome may include:
Gerstmann Syndrome is not believed to be passed on genetically - from parents to their offspring.
The signs and symptoms of Gerstmann Syndrome often vary from one individual to another. It may include any combination of two, or all of these symptoms:
Additional symptoms that may be present, but are less common include:
In children, the disorder may manifest as difficulty in the following:
A diagnosis of Gerstmann Syndrome may include:
Many clinical conditions may have similar signs and symptoms. Your healthcare provider may perform additional tests to rule out other clinical conditions to arrive at a definitive diagnosis.
Possible complications of Gerstmann Syndrome include:
The treatment measures for Gerstmann Syndrome may include:
The measures that may be taken to reduce one’s risk for Gerstmann Syndrome include:
Dr. Josef Gerstmann, a neurologist, characterized the condition in 1924, after whom it is named Gerstmann Syndrome.
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