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Gordon Syndrome

Gordon Syndrome: Introduction

Gordon Syndrome: A genetic musculoskeletal disorder characterized mainly by camptodactyly, cleft palate and club foot. The type and severity of symptoms is variable. More detailed information about the symptoms, causes, and treatments of Gordon Syndrome is available below.

Symptoms of Gordon Syndrome

Wrongly Diagnosed with Gordon Syndrome?

Gordon Syndrome: Related Patient Stories

Gordon Syndrome: Complications

Read more about complications of Gordon Syndrome.

Causes of Gordon Syndrome

Read more about causes of Gordon Syndrome.

Disease Topics Related To Gordon Syndrome

Research the causes of these diseases that are similar to, or related to, Gordon Syndrome:

Less Common Symptoms of Gordon Syndrome

Misdiagnosis and Gordon Syndrome

Leg cramps at night a classic sign: The symptom of having leg muscle cramps, particularly at night, is a classic sign of undiagnosed diabetes. However, there are also various other causes. See causes more »

Gordon Syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for Gordon Syndrome

Medical research articles related to Gordon Syndrome include:

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

Gordon Syndrome: Animations

Research about Gordon Syndrome

Visit our research pages for current research about Gordon Syndrome treatments.

Statistics for Gordon Syndrome

Gordon Syndrome: Broader Related Topics

User Interactive Forums

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

Definitions of Gordon Syndrome:

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


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