Cerebellar Hypoplasia Tapetoretinal Degeneration

Common Name(s)

Cerebellar Hypoplasia Tapetoretinal Degeneration

Cerebellar Hypoplasia Tapetoretinal Degeneration is a rare birth condition characterized by an underdeveloped cerebellum (the part of the brain that controls muscle coordination and balance), and a retinal disorder (eye disorder). Symptoms may include: delayed motor or language development, visual loss, blindness, optic nerve damage (the optic nerve transmits signals from the eyes to the brain), and lack of muscle movement during involuntary movement such as walking (ataxia). Treatment varies on a case-by-case basis.

Source: Advocacy organizations associated with the condition.

 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Cerebellar Hypoplasia Tapetoretinal Degeneration" for support, advocacy or research.

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General Support Organizations

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How do you compare to others with this condition?

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Cerebellar Hypoplasia Tapetoretinal Degeneration" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Cerebellar Hypoplasia Tapetoretinal Degeneration" returned 0 free, full-text research articles on human participants.

Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Cerebellar Hypoplasia Tapetoretinal Degeneration" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.