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Klippel-Feil syndrome recessive type

Klippel-Feil syndrome recessive type: Introduction

Klippel-Feil syndrome recessive type: A rare recessively inherited 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 recessive type is available below.

Symptoms of Klippel-Feil syndrome recessive type

Wrongly Diagnosed with Klippel-Feil syndrome recessive type?

Klippel-Feil syndrome recessive type: Related Patient Stories

Klippel-Feil syndrome recessive type: Complications

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Causes of Klippel-Feil syndrome recessive type

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Klippel-Feil syndrome recessive type: Research Doctors & Specialists

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Klippel-Feil syndrome recessive type: Animations

Statistics for Klippel-Feil syndrome recessive type

Klippel-Feil syndrome recessive type: Broader Related Topics

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Definitions of Klippel-Feil syndrome recessive type:

Klippel-Feil syndrome recessive type 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 recessive type, or a subtype of Klippel-Feil syndrome recessive type, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

 

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