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Diseases » Corpus callosum agenesis » Introduction
 

Corpus callosum agenesis

Corpus callosum agenesis: Introduction

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.

Symptoms of Corpus callosum agenesis

See full list of 14 symptoms of Corpus callosum agenesis

Wrongly Diagnosed with Corpus callosum agenesis?

Causes of Corpus callosum agenesis

See full list of 19 causes of Corpus callosum agenesis

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Evidence Based Medicine Research for Corpus callosum agenesis

Medical research articles related to Corpus callosum agenesis include:

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Prognosis for Corpus callosum agenesis

Prognosis for Corpus callosum agenesis: a few cases are asymptomatic and all cases generally have a normal life span

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Reseach about Corpus callosum agenesis

Visit our research pages for current research about Corpus callosum agenesis treatments.

Stories from Users Related to Corpus callosum agenesis

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Definitions of Corpus callosum agenesis:

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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