Klippel-Feil syndrome

Last revised by Arlene Campos on 11 Jan 2024

Klippel-Feil syndrome is a complex heterogeneous entity that results in cervical vertebral fusion. Two or more non-segmented cervical vertebrae are usually sufficient for diagnosis.

There is a recognized female predilection 1. Klippel-Feil syndrome has an incidence of 1:40,000-42,000 2.

The classic clinical triad of a short neck, low hairline, and restricted neck motion is considered to be present in <50% of patients with this syndrome.

It is believed to result from faulty segmentation along the embryo’s developing axis during the 3rd to 8th weeks of gestation.

There are two classifications:

1.  Original classification (described by Maurice Klippel and Andre Feil): three types grouped depending on the extent and location of vertebral fusion as well as associated vertebral abnormalities 2:

  • type I: fusion of many cervical and upper thoracic vertebrae

  • type II: fusion of two or three vertebrae with associated hemivertebrae, occipito-atlantal fusion or other cervical spine abnormalities

  • type III: cervical fusion with lower thoracic or lumbar vertebral fusion

2. Updated classification (by Clarke et al. 6) grouped by patterns of inheritance, associated anomalies, and the axial level of the most anterior fusion.

On flexion/extension radiographs, there will be less movement between fused segments, and increased movement between non-fused portions.

CT is able to better image many of the features seen on plain radiography and in addition may demonstrate canal stenosis. Central canal narrowing is generally associated with secondary degenerative changes. It is a valuable tool to assess bony anatomy and is very helpful in pre-operative planning.

MRI is indicated in patients with neurologic deficits. It is excellent in demonstrating canal stenosis and cord compression. Disc bulge and herniation can be identified that may encroach upon and damage the spinal cord. MR imaging can also reveal associated conditions such as myelomalacia, syringohydromyelia, diastematomyelia, diplomyelia, and Chiari I malformation 4,5. Associated cord abnormalities are seen in 12% of cases 5.

No definitive treatment exists. Lifestyle modifications and preventive activities include avoidance of contact sports such as rugby. Neck braces and traction may provide symptomatic relief. Adverse sequelae such as pain despite conservative management and progressive instability may benefit from surgical decompression, with or without fusion.

The classic clinical triad in Klippel-Feil syndrome was originally described by Maurice Klippel and Andre Feil in 1912 2.

Differential considerations for the fused appearances of the cervical spine include:

ADVERTISEMENT: Supporters see fewer/no ads