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Ehlers-Danlos syndrome, 6B

Ehlers-Danlos syndrome, 6B: Introduction

Ehlers-Danlos syndrome, 6B: A rare genetic connective tissue disorder characterized by lax joints, scoliosis and fragile sclera of the eye - Ehlers Danlos type with predominant ocular abnormalities but lysyl-hydroxylase activity is normal1. More detailed information about the symptoms, causes, and treatments of Ehlers-Danlos syndrome, 6B is available below.

Symptoms of Ehlers-Danlos syndrome, 6B

Home Diagnostic Testing

Home medical testing related to Ehlers-Danlos syndrome, 6B:

Wrongly Diagnosed with Ehlers-Danlos syndrome, 6B?

Ehlers-Danlos syndrome, 6B: Related Patient Stories

Causes of Ehlers-Danlos syndrome, 6B

Read more about causes of Ehlers-Danlos syndrome, 6B.

Disease Topics Related To Ehlers-Danlos syndrome, 6B

Research the causes of these diseases that are similar to, or related to, Ehlers-Danlos syndrome, 6B:

Ehlers-Danlos syndrome, 6B: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Ehlers-Danlos syndrome, 6B

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Ehlers-Danlos syndrome, 6B: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Ehlers-Danlos syndrome, 6B: Animations

Statistics for Ehlers-Danlos syndrome, 6B

Ehlers-Danlos syndrome, 6B: Broader Related Topics

User Interactive Forums

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Definitions of Ehlers-Danlos syndrome, 6B:

Ehlers-Danlos syndrome, 6B is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Ehlers-Danlos syndrome, 6B, or a subtype of Ehlers-Danlos syndrome, 6B, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

 

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