Is Klippel-Feil Syndrome painful?

Is Klippel-Feil Syndrome painful?

Klippel-Feil syndrome (KFS) symptoms can range from minor discomfort to severe pain and limited range of motion in the neck.

Is Klippel-Feil Syndrome life expectancy?

In less than 30% of cases, individuals with KFS will present with heart defects. If these heart defects are present, they often lead to a shortened life expectancy, the average being 35–45 years of age among males and 40–50 among females. This condition is similar to the heart failure seen in gigantism.

Is Klippel-Feil Syndrome a disability?

If you or your dependent(s) are diagnosed with Klippel-Feil Syndrome and experience any of these symptoms, you may be eligible for disability benefits from the U.S. Social Security Administration.

Is Klippel-Feil curable?

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.

Can Klippel-Feil syndrome cause headaches?

In people with Klippel-Feil syndrome, the fused vertebrae can limit the range of movement of the neck and back as well as lead to chronic headaches and muscle pain in the neck and back that range in severity.

Is it possible to 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.

What is short neck?

Klippel-Feil Syndrome: Short Neck and Congenital Cervical Spine Disorder. Written by Kelly Rehan. 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.

Who gets Klippel-Feil syndrome?

Klippel-Feil syndrome is estimated to occur in 1 in 40,000 to 42,000 newborns worldwide. Females seem to be affected slightly more often than males.

What is it called when you have no neck?

Can Klippel Feil syndrome cause headaches?

Are you born with Klippel Feil syndrome?

Klippel-Feil syndrome forms in utero when genes GDF6 or GDF3 mutate. The condition is present at birth, but it may go undetected for years if the symptoms are slight. Some children with Klippel-Feil syndrome won’t be diagnosed with vertebral problems until an accident causes pain or worsens the symptoms.

What to know about Klippel-Feil syndrome?

Klippel-Feil syndrome ( KFS ), also known as cervical vertebral fusion syndrome, is a rare congenital condition characterized by the abnormal fusion of any two of the seven bones in the neck ( cervical vertebrae ). It results in a limited ability to move the neck and shortness of the neck, resulting in the appearance of a low hairline.

How does Klippel Feil syndrome affect people?

Klippel Feil syndrome (KFS) is a condition affecting the development of the bones in the spine . 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.

What is the history of Klippel-Feil syndrome?

Klippel-Feil syndrome is estimated to occur in 1 out of every 40,000 births. It was first identified in 1912 by Frenchmen Maurice Klippel and André Feil. Klippel-Feil syndrome forms in utero when genes GDF6 or GDF3 mutate. The condition is present at birth, but it may go undetected for years if the symptoms are slight.

What is Klippel-Feil syndrome?

General Discussion. Klippel-Feil syndrome (KFS) is a rare skeletal disorder primarily characterized by abnormal union or fusion of two or more bones of the spinal column (vertebrae) within the neck (cervical vertebrae).