44 rows · Aug 04, 2017 · Klippel Feil syndrome (KFS) is a congenital, musculoskeletal condition characterized by the fusion of at least two vertebrae of the neck. Common symptoms include a short neck, low hairline at the back of the head, and restricted mobility of the upper spine. This syndrome can cause chronic headaches as well as pain in both the neck and the back. Less than half of all individuals with Klippel-Feil syndrome have all three classic features of this condition. 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. People with minimal bone involvement often have fewer problems compared to individuals .
Sep 10, 2014 · Extremely limited range of motion of the cervical spine. Range of Motion- People with Klippel-Feil Syndrome have limited range of motion of the cervical spine due to abnormal fusion of the vertebrae. Radicular Pain- Patient suffers with severe pain. Pain Occupation: MD,FFARCSI. Many people with Klippel-Feil syndrome have abnormal side-to-side curvature of the spine (scoliosis) due to malformation of the vertebrae; fusion of additional vertebrae below the neck may also occur. People with Klippel-Feil syndrome may have a wide variety .
The hope of living with Klippel Feil depends on the associated abnormalities specific that may affect the patient and the type of syndrome. Recent studies indicate that those individuals diagnosed with a mild form of this rare condition have a life expectancy similar to that of the general population. Subdivisions of Klippel-Feil Syndrome. KFS may occur as an isolated abnormality or in association with certain syndromes. In many individuals with KFS, the condition appears to occur randomly for unknown reasons (sporadically). In other cases, KFS may be inherited as an autosomal dominant or autosomal .
Klippel-Feil syndrome is an uncommon condition that is present from birth and which features the fusion of any two of the seven cervical vertebrae. It can be said that Klippel-Feil syndrome is present in a heterogeneous bunch of individuals, who are united only by the prevalence of a congenital abnormality in the segmentation or development of the cervical spine. KLIPPEL-FEIL SYNDROME. Klippel-Feil Syndrome is an uncommon congenital fusion of the Cervical Vertebrae, whether it involves 2 segments, congenital block vertebrae, or the entire Cervical Spine. Congenital Cervical fusion is the result of failure of normal segmentation of the cervical bone precursors (called "somites") during the third to eighth weeks of life.
Klippel-Feil Syndrome Prognosis. According to the statistics gathered, persons having Klippel Feil syndrome will usually live for a maximum of 25 years of age. Yet, some of the persons with this kind of syndrome have normal prognosis or life span. The prognosis is considered good if there is only mild form of this kind of syndrome. Klippel–Feil syndrome (KFS), also known as cervical vertebral fusion syndrome, is a rare condition present at birth (congenital disease) characterized by the abnormal joining of any two of the seven bones in the neck (cervical vertebrae).: 578 It results in a limited ability to move the neck and shortness of the neck resulting in the appearance of a low hairline.Causes: Genetic mutations.