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
See full list of 12
symptoms of Gordon Syndrome
Gordon Syndrome: Complications
Read more about complications of Gordon Syndrome.
Disease Topics Related To Gordon Syndrome
Research the causes of these diseases that are similar to, or related to, Gordon Syndrome:
Medical Textbooks Online about Gordon Syndrome
Medical Books Excerpts
- Clubbing
- "In A Page: Pediatric Signs and Symptoms" (2007)
- [ read ]
- Clubbing
- "Handbook of Signs & Symptoms (Third Edition)" (2006)
- [ read ]
- Clubbing
- "A Pocket Manual of Differential Diagnosis" (1999)
- [ read ]
- Clubfoot
- "Professional Guide to Diseases (Eighth Edition)" (2005)
- [ read ]
- Clubbing
- "Professional Guide to Signs & Symptoms (Fifth Edition)" (2006)
- [ read ]
- Clubbing
- "Nursing: Interpreting Signs and Symptoms" (2007)
- [ read ]
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Less Common Symptoms of Gordon Syndrome
Read more about symptoms of Gordon Syndrome
Wrongly Diagnosed with Gordon Syndrome?
Causes of Gordon Syndrome
Read more about causes of Gordon Syndrome.
News Archives for Gordon Syndrome
Medical news articles related to Gordon Syndrome include:
Source: HealthDay News
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
Videos for Gordon Syndrome
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See full list of 4 related videos
Reseach about Gordon Syndrome
Visit our research pages for current research about Gordon Syndrome treatments.
Stories from Users Related to Gordon Syndrome
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
Contents for Gordon Syndrome:
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