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Behr syndrome

Behr syndrome: Introduction

Behr syndrome: A rare inherited neurological condition characterized by spastic paraplegia and sometimes optic atrophy. More detailed information about the symptoms, causes, and treatments of Behr syndrome is available below.

Symptoms of Behr syndrome

Home Diagnostic Testing

Home medical testing related to Behr syndrome:

Wrongly Diagnosed with Behr syndrome?

Behr syndrome: Complications

Read more about complications of Behr syndrome.

Causes of Behr syndrome

Read more about causes of Behr syndrome.

Disease Topics Related To Behr syndrome

Research the causes of these diseases that are similar to, or related to, Behr syndrome:

Behr syndrome: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Behr syndrome

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as more »

Behr syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Behr syndrome: Animations

Statistics for Behr syndrome

Behr syndrome: Broader Related Topics

User Interactive Forums

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

Definitions of Behr syndrome:

Ataxia, optic atrophy, neurologic signs, mental retardation, spinocerebellar degeneration, and visual disorders. - (Source - Diseases Database)

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


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