Definition. 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.
When Klippel-Feil syndrome is caused by mutations in the GDF6 or GDF3 genes, it is inherited in an autosomal dominant pattern , which means one copy of the altered gene in each cell is sufficient to cause the disorder.
Surgical treatment was performed for Klippel–Feil syndrome with severe basilar invagination. Basilar invagination could not be reduced by conservative combination treatment using a halo vest and direct traction. Gentle intraoperative reduction achieved good spinal alignment and reduction of basilar invagination.
Q32. 3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM Q32. 3 became effective on October 1, 2021.
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.
Genetic testing. If at least 2 cervical vertebrae are fused and other aspects of the exam signal that the condition is congenital (from birth), Klippel-Feil syndrome is diagnosed.
Some cases of KFS can become serious and potentially life-threatening in a few different ways: Cervical myelopathy. If the spinal cord starts to become compressed, such as from bony overgrowths or severe spinal deformity, problems with coordination and reduced control over bodily functions could result.
Klippel-Feil syndrome (KFS) symptoms can range from minor discomfort to severe pain and limited range of motion in the neck. Other conditions may occur with KFS, and the symptoms associated with these other conditions can also run the spectrum in terms of severity and whether or not they impact quality of life.
Surgery for KFS There are numerous surgical treatment possibilities for conditions that may accompany KFS. For example, a plastic surgeon may perform surgery for cleft palate (closing a split in the roof of the mouth), or a cardiovascular surgeon may perform heart surgery.
M48. 061 Spinal stenosis, lumbar region without neurogenic claud - ICD-10-CM Diagnosis Codes.
02: Spinal stenosis Cervical region.
Congenital spinal stenosis: This is a condition in which a person is born with a small spinal canal. Another congenital spinal deformity that can put a person at risk for spinal stenosis is scoliosis (an abnormally shaped spine).
The ICD code Q761 is used to code Klippel-Feil syndrome. Klippel–Feil syndrome is a rare disease, initially reported in 1912 by Maurice Klippel and André Feil from France, characterized by the congenital fusion of any two of the seven cervical vertebrae.:578 . The syndrome occurs in a heterogeneous group of patients unified only by the presence ...
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis. The Center for Medicare & Medicaid Services (CMS) requires medical coders to indicate whether or not a condition was present at the time of admission, in order to properly assign MS-DRG codes.