![]() How can I or my loved one help improve care for people with Klippel-Feil syndrome? The outlook depends on the severity of the case and on the number of related conditions a person has. It is possible for people with Klippel-Feil syndrome to live normal lives with proper treatment and care. People with Klippel-Feil syndrome should avoid activities that can injure the neck. You may see many types of doctors to treat other symptoms. Tests may be performed to learn if the disorder is mild or severe.ĭoctors currently treat Klippel-Feil syndrome with surgery to correct the neck bones. Mutations in the GDF6 (growth differentiation factor 6) or GDF3 (growth differentiation factor 3) genes can cause the disorder.ĭoctors usually diagnose Klippel-Feil syndrome at or near birth through observation. ![]() People with a certain genetic mutation are at higher risk of developing the disorder. Hearing loss-Sound signals have a hard time getting to the right part of the ear or brain.Pain-The fused vertebrae can cause nerve damage and pain in the head, neck, or back.Limited flexibility and movement, affecting the face, neck, upper body, and back.Short neck and the potential for a low hairline at the back of the head.The most common symptoms of Klippel-Feil syndrome include: People living with Klippel-Feil syndrome may have a short neck limited movement, and pain. ![]() Klippel-Feil syndrome is a rare disorder where two or more vertebrae in the neck are fused together from birth. ![]()
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