Short Neck Syndrome

Short neck syndrome is a rare hereditary disease that is associated with impaired development of the cervical spine. This disease manifests itself in the formation of short and tight cervical vertebrae, which leads to shortening of the neck and difficulty moving the head.

Short neck syndrome is also known as Klinpel-Felli tumor, and this is not only a medical problem, but also a social problem, since the diagnosis of “Short neck syndrome” is determined by the anatomical and physiological state of the cervical segment and the characteristics of its development, and requires treatment aimed at improving quality of life of the patient and to prevent the development of complications.

Treatment of short neck syndrome begins with timely identification of the disease and the choice of individual treatment depending on the patient’s age, the nature of the disease, the severity of changes in the spine and associated disorders. This may include surgery to correct and lengthen the neck area, orthopedic devices to support the head and neck, and, if necessary, injections of growth hormones. Physiotherapy, massage, and medication may also be helpful to relieve underlying symptoms and improve the patient's overall condition.

As the patient's age grows, the health condition worsens and various functional disorders occur in health and life. During the period when the spine becomes rigid, the center of gravity shifts when sitting vertically and downward, the position of the head changes, scoliosis occurs, facial pathology, chest deformation, and so on. Symptoms that appear in childhood and adolescence continue to progress into adulthood, negatively impacting quality of life, daily activities, and adjustment to life among healthy individuals. The presence of Short Neck Syndrome can change the natural course of life - constant adjustment is required depending on the need to adapt to the necessary requirements.