Does Klippel-Feil syndrome get worse with age?

KFS symptoms may or may not be apparent at birth or during childhood. However, KFS symptoms typically worsen with age and may become more apparent later in life.

Is Klippel-Feil syndrome life threatening?

When Klippel-Feil Syndrome Is Serious Some cases of KFS can become serious and potentially life-threatening in a few different ways: Cervical myelopathy.

Does Klippel-Feil syndrome affect the brain?

Rarely, structural brain abnormalities or a type of birth defect that occurs during the development of the brain and spinal cord (neural tube defect) can occur in people with Klippel-Feil syndrome.

Can Klippel-Feil syndrome be fixed?

There is no cure for Klippel-Feil syndrome. Treatment is ordered when certain issues — such as spinal curvatures, muscle weaknesses or heart problems — occur and need to be treated.

Is Klippel Feil 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.

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.

Is Klippel Feil syndrome a disability?

Is Klippel Feil syndrome a rare disease?

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).

Can fused vertebrae be corrected?

Fusion is used to correct problems with the small bones of the spine. t’s almost like a welding process where the painful vertebrae are fused together so they can heal into a single solid bone.

What’s the prognosis for Klippel Feil syndrome?

The long-term outlook (prognosis) for people with Klippel Feil syndrome varies depending on the specific features and severity in each affected person. While all affected people have fusion of at least two vertebrae of the neck, additional signs and symptoms (if present) can vary greatly 5).

How did Klippel Feil syndrome get its name?

With such condition, the neck and spinal movement are restricted. It is sometimes associated with abnormalities in the patient’s organ. This kind of syndrome is of rare occurrence. Its name was given in honor of the ones who discover it namely, Maurice Klippel and Andre Feil resulting to the name Klippel-Feil syndrome.

What kind of Doctor do you see for Klippel Feil?

Prescription of the medical therapy is based on the abnormalities that the person possesses. If you have auditory abnormalities, you need to consult the audiologist. Or for instance, persons with cardiovascular abnormalities will need the help of the cardiologist expert for their medical therapy treatment.

Where does the fusion in Klippel Feil occur?

The fusion happens in the C2 or cervical vertebrae bone number 2 and C7 or cervical vertebrae bone number 7. It is due to the failed normal division or segmentation of the person’s cervical vertebrae which is upon the early fetal developmental stage.

What is the prognosis for Klippel Feil syndrome?

Prognosis. The long-term outlook ( prognosis) for people with Klippel Feil syndrome varies depending on the specific features and severity in each affected person. While all affected people have fusion of at least two vertebrae of the neck, additional signs and symptoms (if present) can vary greatly.

With such condition, the neck and spinal movement are restricted. It is sometimes associated with abnormalities in the patient’s organ. This kind of syndrome is of rare occurrence. Its name was given in honor of the ones who discover it namely, Maurice Klippel and Andre Feil resulting to the name Klippel-Feil syndrome.

Is it possible for only one identical twin to have Klippel Feil syndrome?

Is it possible for only one identical twin to have Klippel Feil syndrome? It is theoretically possible for only one identical (monozygotic) twin to have Klippel Feil syndrome. While both autosomal and recessive inheritance patterns have been described, most cases of Klippel Feil syndrome are sporadic.

How are EOS images used to diagnose Klippel Feil syndrome?

Unlike a CT scan, EOS images are taken while the child is in an upright or standing position, enabling improved diagnosis due to weight-bearing positioning. Children with Klippel-Feil syndrome may have other health issues too, such as kidney, heart or lung problems.