Klippel-Feil syndrome, dominant type: A rare dominantly 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, dominant type is available below.
See full list of 29 symptoms of Klippel-Feil syndrome, dominant type
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Klippel-Feil syndrome, dominant 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, dominant type, or a subtype of Klippel-Feil syndrome, dominant type,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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