Corpus Callosum Agenesis

Below you will find more information about Corpus Callosum Agenesis from Medigest. If you believe that you are suffering from any of the symptoms of Corpus Callosum Agenesis 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 Corpus Callosum Agenesis 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 Corpus Callosum Agenesis comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Corpus callosum agenesis is an uncommon congenital disorder, wherein there's a partial or complete absence of an area of the brain that connects its two cerebral hemispheres known as 'corpus callosum'.


An effective method for diagnosing Corpus callosum agenesis is through brain scan. Other methods include CT scan, MRI, prenatal MRI, and prenatal ultrasound.


Currently, there are no particular medical treatments for the disorder, but affected individuals can benefit from a variety of educational support, services, and developmental therapies. It's important to seek medical advice from specialists, such s neurologists, physical therapists, geneticists, occupational therapists, and others.

Symptoms and Signs

The symptoms of the disorder vary greatly from person to person. However, there are some common symptoms in affected individuals including hypotonia or low tone of the muscle, vision impairments, reduced motor coordination, swallowing and chewing difficulties, early language and speech delays, low discernment of pain, social difficulties, and motor milestones delays like walking and sitting.


Corpus callosum agenesis results from development disruption of the 'fetal brain' during its fifth and sixth week of conception. The cause of this disruption is unknown; however, some studies suggest that a number of possible causes can include inherited genetic defect, chromosome errors, prenatal injuries or infections, prenatal exposure to toxins, and metabolic disorders.

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