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Fitzsimmons-Guilbert syndrome

Fitzsimmons-Guilbert syndrome: Introduction

Fitzsimmons-Guilbert syndrome: A very rare syndrome characterized mainly by paraplegia, short fingers and bone abnormalities. The paraplegia progresses slowly. More detailed information about the symptoms, causes, and treatments of Fitzsimmons-Guilbert syndrome is available below.

Symptoms of Fitzsimmons-Guilbert syndrome

Home Diagnostic Testing

Home medical testing related to Fitzsimmons-Guilbert syndrome:

Wrongly Diagnosed with Fitzsimmons-Guilbert syndrome?

Fitzsimmons-Guilbert syndrome: Related Patient Stories

Fitzsimmons-Guilbert syndrome: Complications

Read more about complications of Fitzsimmons-Guilbert syndrome.

Causes of Fitzsimmons-Guilbert syndrome

Read more about causes of Fitzsimmons-Guilbert syndrome.

Disease Topics Related To Fitzsimmons-Guilbert syndrome

Research the causes of these diseases that are similar to, or related to, Fitzsimmons-Guilbert syndrome:

Fitzsimmons-Guilbert syndrome: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Fitzsimmons-Guilbert syndrome

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis). See symptoms...read more »

Fitzsimmons-Guilbert syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Fitzsimmons-Guilbert syndrome: Animations

Statistics for Fitzsimmons-Guilbert syndrome

Fitzsimmons-Guilbert syndrome: Broader Related Topics

User Interactive Forums

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

Definitions of Fitzsimmons-Guilbert syndrome:

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

 

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