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Klippel Feil Syndrome



Klippel Feil Syndrome: Introduction

Klippel Feil Syndrome: Klippel-Feil syndrome is a rare disorder defined as the congenital fusion of any 2 of the 7 cervical (neck) vertebrae. It is caused by a failure in the ... more about Klippel Feil Syndrome.

Klippel Feil Syndrome: A rare congenital disorder characterized by abnormal fusion of two or more vertebrae in the neck. The disorder is often associated with other abnormalities but their incidence is highly variable. More detailed information about the symptoms, causes, and treatments of Klippel Feil Syndrome is available below.

Symptoms of Klippel Feil Syndrome

See full list of 33 symptoms of Klippel Feil Syndrome

Klippel Feil Syndrome: Complications

Review possible medical complications related to Klippel Feil Syndrome:

Medical Textbooks Online about Klippel Feil Syndrome

Medical Books Excerpts
  • "Professional Guide to Diseases (Eighth Edition)" (2005)
  • "Professional Guide to Diseases (Eighth Edition)" (2005)
  • "Professional Guide to Diseases (Eighth Edition)" (2005)
  • "Handbook of Diseases" (2003)
  • "Handbook of Diseases" (2003)
  • "The 5-Minute Pediatric Consult" (2008)
  • "Pediatric Infectious Disease" (2004)

Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

Wrongly Diagnosed with Klippel Feil Syndrome?

Klippel Feil Syndrome: Marketplace Products, Discounts & Offers

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Klippel Feil Syndrome: Research Doctors & Specialists

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Causes of Klippel Feil Syndrome

Read more about causes of Klippel Feil Syndrome.

Treatments for Klippel Feil Syndrome

Read more about treatments for Klippel Feil Syndrome

News Archives for Klippel Feil Syndrome

Medical news articles related to Klippel Feil Syndrome include:

Source: HealthDay News

Evidence Based Medicine Research for Klippel Feil Syndrome

Medical research articles related to Klippel Feil Syndrome include:

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

Videos for Klippel Feil Syndrome

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Patient Surveys for Klippel Feil Syndrome

Prognosis for Klippel Feil Syndrome

Prognosis for Klippel Feil Syndrome: Usually good.

More about prognosis of Klippel Feil Syndrome

Reseach about Klippel Feil Syndrome

Visit our research pages for current research about Klippel Feil Syndrome treatments.

Statistics for Klippel Feil Syndrome

Klippel Feil Syndrome: Broader Related Topics

Types of Klippel Feil Syndrome

Stories from Users Related to Klippel Feil Syndrome

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Article Excerpts about Klippel Feil Syndrome

Klippel-Feil syndrome is a rare disorder defined as the congenital fusion of any 2 of the 7 cervical (neck) vertebrae. It is caused by a failure in the normal segmentation or division of the cervical vertebrae during the early weeks of fetal development. (Source: excerpt from NINDS Klippel Feil Syndrome Information Page: NINDS)

Definitions of Klippel Feil Syndrome:

A condition characterized by shortness of the neck resulting from reduction in the number of vertebrae or the fusion of multiple hemivertebrae into one osseous mass. The hairline is low and the motion of the neck is limited. (Dorland, 27th ed) - (Source - Diseases Database)

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


 » Next page: What is Klippel Feil Syndrome?

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