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Apraxia, oculomotor, Cogan type

Apraxia, oculomotor, Cogan type: Introduction

Apraxia, oculomotor, Cogan type: A rare inherited condition where the person is unable to move eyes horizontally making it difficult to follow objects. More detailed information about the symptoms, causes, and treatments of Apraxia, oculomotor, Cogan type is available below.

Symptoms of Apraxia, oculomotor, Cogan type

Home Diagnostic Testing

Home medical testing related to Apraxia, oculomotor, Cogan type:

Wrongly Diagnosed with Apraxia, oculomotor, Cogan type?

Apraxia, oculomotor, Cogan type: Related Patient Stories

Apraxia, oculomotor, Cogan type: Deaths

Read more about Deaths and Apraxia, oculomotor, Cogan type.

Causes of Apraxia, oculomotor, Cogan type

Read more about causes of Apraxia, oculomotor, Cogan type.

More information about causes of Apraxia, oculomotor, Cogan type:

Disease Topics Related To Apraxia, oculomotor, Cogan type

Research the causes of these diseases that are similar to, or related to, Apraxia, oculomotor, Cogan type:

Apraxia, oculomotor, Cogan type: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Apraxia, oculomotor, Cogan type: Research Doctors & Specialists

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Apraxia, oculomotor, Cogan type: Animations

Statistics for Apraxia, oculomotor, Cogan type

Apraxia, oculomotor, Cogan type: Broader Related Topics

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Definitions of Apraxia, oculomotor, Cogan type:

Apraxia, oculomotor, Cogan type is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Apraxia, oculomotor, Cogan type, or a subtype of Apraxia, oculomotor, Cogan type, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Apraxia, oculomotor, Cogan type as a "rare disease".
Source - Orphanet

 

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