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Ehlers Danlos syndrome type 4, autosomal dominant

Ehlers Danlos syndrome type 4, autosomal dominant: Introduction

Ehlers Danlos syndrome type 4, autosomal dominant: A rare genetic connective tissue disorder characterized by delicate skin, fragile blood vessels, distinctive facial features and minimal joint problems - previously known as EDS type 4. More detailed information about the symptoms, causes, and treatments of Ehlers Danlos syndrome type 4, autosomal dominant is available below.

Symptoms of Ehlers Danlos syndrome type 4, autosomal dominant

Wrongly Diagnosed with Ehlers Danlos syndrome type 4, autosomal dominant?

Ehlers Danlos syndrome type 4, autosomal dominant: Related Patient Stories

Ehlers Danlos syndrome type 4, autosomal dominant: Complications

Review possible medical complications related to Ehlers Danlos syndrome type 4, autosomal dominant:

Causes of Ehlers Danlos syndrome type 4, autosomal dominant

Read more about causes of Ehlers Danlos syndrome type 4, autosomal dominant.

Misdiagnosis and Ehlers Danlos syndrome type 4, autosomal dominant

Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer from the skin disorder called psoriasis can often go undiagnosed. The main problem is...read more »

Psoriatic arthritis often undiagnosed cause of joint conditions: Patients with the skin condition psoriasis can also have the related arthritis subtype called " psoriatic...read more »

Ehlers Danlos syndrome type 4, autosomal dominant: Research Doctors & Specialists

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Ehlers Danlos syndrome type 4, autosomal dominant: Animations

Statistics for Ehlers Danlos syndrome type 4, autosomal dominant

Ehlers Danlos syndrome type 4, autosomal dominant: Broader Related Topics

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Definitions of Ehlers Danlos syndrome type 4, autosomal dominant:

Ehlers Danlos syndrome type 4, autosomal dominant 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 type 4, autosomal dominant, or a subtype of Ehlers Danlos syndrome type 4, autosomal dominant, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

 

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