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COFS syndrome

COFS syndrome: Introduction

COFS syndrome: A genetic disorder involving degeneration of the brain and spinal cord that starts during the fetal stage. More detailed information about the symptoms, causes, and treatments of COFS syndrome is available below.

Symptoms of COFS syndrome

Home Diagnostic Testing

Home medical testing related to COFS syndrome:

Wrongly Diagnosed with COFS syndrome?

COFS syndrome: Related Patient Stories

Causes of COFS syndrome

Read more about causes of COFS syndrome.

COFS syndrome: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and COFS syndrome

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COFS syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

COFS syndrome: Rare Types

Rare types of diseases and disorders in related medical categories:

Evidence Based Medicine Research for COFS syndrome

Medical research articles related to COFS syndrome include:

Click here to find more evidence-based articles on the TRIP Database

COFS syndrome: Animations

Research about COFS syndrome

Visit our research pages for current research about COFS syndrome treatments.

Statistics for COFS syndrome

COFS syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about COFS syndrome, or answer someone else's question, on our message boards:

Definitions of COFS syndrome:

COFS syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that COFS syndrome, or a subtype of COFS syndrome, 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 COFS syndrome as a "rare disease".
Source - Orphanet

 

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