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Freeman-Sheldon Syndrome

Freeman-Sheldon Syndrome: Introduction

Freeman-Sheldon Syndrome: A very rare genetic disorder characterized by abnormal development of the skeleton and muscles. More detailed information about the symptoms, causes, and treatments of Freeman-Sheldon Syndrome is available below.

Symptoms of Freeman-Sheldon Syndrome

Wrongly Diagnosed with Freeman-Sheldon Syndrome?

Freeman-Sheldon Syndrome: Related Patient Stories

Freeman-Sheldon Syndrome: Complications

Review possible medical complications related to Freeman-Sheldon Syndrome:

Causes of Freeman-Sheldon Syndrome

Read more about causes of Freeman-Sheldon Syndrome.

Disease Topics Related To Freeman-Sheldon Syndrome

Research the causes of these diseases that are similar to, or related to, Freeman-Sheldon Syndrome:

Less Common Symptoms of Freeman-Sheldon Syndrome

Misdiagnosis and Freeman-Sheldon Syndrome

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

Freeman-Sheldon Syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for Freeman-Sheldon Syndrome

Medical research articles related to Freeman-Sheldon Syndrome include:

Click here to find more evidence-based articles on the TRIP Database

Freeman-Sheldon Syndrome: Animations

Research about Freeman-Sheldon Syndrome

Visit our research pages for current research about Freeman-Sheldon Syndrome treatments.

Statistics for Freeman-Sheldon Syndrome

Freeman-Sheldon Syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Freeman-Sheldon Syndrome, or answer someone else's question, on our message boards:

Definitions of Freeman-Sheldon Syndrome:

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

 

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