Best answer: Can people have short spine syndrome?

Klippel-Feil Syndrome: Short Neck and Congenital Cervical Spine Disorder. Klippel-Feil syndrome (KFS) occurs when two or more vertebrae in your neck (cervical spine) are abnormally fused together. KFS is a congenital disorder, which means you are born with it.

Can humans have short spine syndrome?

People with KFS are born with abnormal fusion of at least two spinal bones (vertebrae) in the neck. Common features may include a short neck, low hairline at the back of the head, and restricted movement of the upper spine. Some people with KFS have no symptoms.

Can a person have no neck?

Klippel-Feil Syndrome (KFS) is a congenital bone condition in which at least 2 cervical vertebrae remain fused and immobile. Some common signs may include a visibly short neck and low hairline behind the head.

Can KFS be fixed?

There is no cure for Klippel-Feil syndrome (KFS), so treatments focus on managing the symptoms. Treatment programs can vary widely, depending on the severity of KFS, as well as any other conditions that might be present.

Do paralyzed dogs have a shorter lifespan?

Can a paralyzed dog live a happy life? The short answer—it depends on the dog’s individual condition and unique health needs. Overall, it’s very possible for a paralyzed or partially paralyzed dog to continue to live a full, happy life.

What is Klippel Feil syndrome?

Klippel-Feil Syndrome is a rare disorder characterized by the congenital fusion of two or more 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.

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Can you have mild Klippel Feil syndrome?

The disorder is present at birth (congenital), but mild cases may go undiagnosed until later during life when symptoms worsen or first become apparent. In some individuals, KFS can be associated with a variety of additional symptoms and physical abnormalities.

Are neck issues hereditary?

Many cervical spine conditions — both common and rare — have a genetic component. Genetic conditions can be caused by inheritance (passed from parent to child), disrupted or abnormal development in utero, or unknown factors. Genetic conditions that affect the cervical spine vary widely.

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