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Corpus callosum agenesis: A very rare congenital abnormality where part or all of the fibers that connect the two halves of the brain (corpus callosum) are missing. More detailed information about the symptoms, causes, and treatments of Corpus callosum agenesis is available below.
See full list of 14 symptoms of Corpus callosum agenesis
See full list of 19 causes of Corpus callosum agenesis
Read more about causes of Corpus callosum agenesis.
More information about causes of Corpus callosum agenesis:
Medical research articles related to Corpus callosum agenesis include:
Click here to find more evidence-based articles on the TRIP Database
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Prognosis for Corpus callosum agenesis: a few cases are asymptomatic and all cases generally have a normal life span
More about prognosis of Corpus callosum agenesis
Visit our research pages for current research about Corpus callosum agenesis treatments.
Read about other experiences, ask a question about Corpus callosum agenesis, or answer someone else's question, on our message boards:
Corpus callosum agenesis is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Corpus callosum agenesis, or a subtype of Corpus callosum agenesis,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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