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Fitzsimmons-McLachlan-Gilbert syndrome

Fitzsimmons-McLachlan-Gilbert syndrome: Introduction

Fitzsimmons-McLachlan-Gilbert syndrome: A very rare syndrome characterized mainly by mental retardation paraplegia and thickened coarse skin on palms and soles. More detailed information about the symptoms, causes, and treatments of Fitzsimmons-McLachlan-Gilbert syndrome is available below.

Symptoms of Fitzsimmons-McLachlan-Gilbert syndrome

Wrongly Diagnosed with Fitzsimmons-McLachlan-Gilbert syndrome?

Fitzsimmons-McLachlan-Gilbert syndrome: Related Patient Stories

Causes of Fitzsimmons-McLachlan-Gilbert syndrome

Read more about causes of Fitzsimmons-McLachlan-Gilbert syndrome.

Misdiagnosis and Fitzsimmons-McLachlan-Gilbert syndrome

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Fitzsimmons-McLachlan-Gilbert syndrome: Research Doctors & Specialists

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Fitzsimmons-McLachlan-Gilbert syndrome: Animations

Statistics for Fitzsimmons-McLachlan-Gilbert syndrome

Fitzsimmons-McLachlan-Gilbert syndrome: Broader Related Topics

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Definitions of Fitzsimmons-McLachlan-Gilbert syndrome:

Fitzsimmons-McLachlan-Gilbert 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-McLachlan-Gilbert syndrome, or a subtype of Fitzsimmons-McLachlan-Gilbert 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-McLachlan-Gilbert syndrome as a "rare disease".
Source - Orphanet

 

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