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Fryns-Hofkens-Fabry syndrome

Fryns-Hofkens-Fabry syndrome: Introduction

Fryns-Hofkens-Fabry syndrome: A very rare syndrome characterized underdeveloped forearm bones. More detailed information about the symptoms, causes, and treatments of Fryns-Hofkens-Fabry syndrome is available below.

Symptoms of Fryns-Hofkens-Fabry syndrome

Wrongly Diagnosed with Fryns-Hofkens-Fabry syndrome?

Fryns-Hofkens-Fabry syndrome: Related Patient Stories

Causes of Fryns-Hofkens-Fabry syndrome

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Fryns-Hofkens-Fabry syndrome: Research Doctors & Specialists

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Statistics for Fryns-Hofkens-Fabry syndrome

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Definitions of Fryns-Hofkens-Fabry syndrome:

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

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More information about Fryns-Hofkens-Fabry syndrome

  1. Fryns-Hofkens-Fabry syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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