Wright Syndrome

Wright's syndrome is a term used to describe a condition where a person experiences pain and discomfort in the lower back and mid-chest area. This condition can be caused by muscle tension, especially the pectoralis minor muscle.

Wright's syndrome was named after the American physician Ivan Simons Wright, who first described it in the 19th century. Wright describes his observations of patients who experienced back and chest pain due to tightness of the pectoralis minor muscle. He also points out that patients with this syndrome often have breathing problems and complaints of coughing.

Since then, Wright's syndrome has become known as pectoralis minor syndrome. This term is used to emphasize that the main cause of the syndrome is tightness of the pectoralis minor muscle, a small muscle located on the side of the chest that allows breathing and movement of the spine.

Wright syndrome symptoms may include:

Pain and discomfort in the pectoralis minor muscle, chest, back, or even neck. Difficulty with deep breathing, feeling of lack of air, pain when exhaling. Problems with swallowing, upper airway obstruction. Palpitations, arrhythmia, most often when trying to take a deep breath or sneeze. Changed head position

Wright syndrome is a neurological disease characterized by peripheral paresis and trophic disorders of the hand. There is a synonym - pectoralis minor syndrome, although this name is not a complete one, but denotes only one of the component manifestations of the disease. It was created for the convenience of doctors and patients. There are a couple of varieties of the syndrome: rigid and spasmodic. In the first case, the muscles almost completely lose elasticity, in the second, on the contrary, they are atrophied or paralyzed, the human body is deformed. Both forms of pathology can be associated with psychological experiences, impaired mental development or personality development.

Wright's syndrome is a neurological pathology that affects both the cerebral cortex and the sensory and motor systems. This is manifested by a disorder of the peripheral nervous system in combination with damage to the pectoralis minor muscles, which is called Wright's syndrome. Pathology occurs against the background of long-term

Wright's syndrome is a benign scoliotic disease of the hip joints, characterized by weakness of extension and supporting function. About 12% of infants have symptoms of this disease; it is rare in adults. Among the main causes of Wright's syndrome are a spasmodic pectoral muscle and a crossed intra-articular ligament. The support is placed on a healthy joint, and the other joint is blocked during fixation, which can lead to muscle wasting. This syndrome most often involves the right lower limb compared to the left, more affected side.

Symptoms characteristic of this syndrome include: 1. Weakness in the extensor activity of the hip extensor (hip muscle), which is unable to lift the knee. The child cannot straighten his knees when lying on his back, touching his foot with one hand and pointing the opposite toe up. 2. Restriction of hip joint motion by approximately 30°, impairment of the passive arch of the foot. A passive arch with support during standing is a sign of knee flexor weakness. 3. Dysfunction of the extensor mechanism of the hip joint, manifested by the inability to abduct the chin. This condition means a weakened ability to rise and fall from a prone position

Wright, Stephen Vincent "White" Syndrome is a rare inherited neuromuscular disorder that is characterized by progressive paralysis of the chest muscles and ultimately leads to death by the age of two to three years. The syndrome was described by doctor i. s Wright in 1948. This name reflects the fact that the patient dies before he reaches adulthood. Wright syndrome is usually associated with defects in the MYH7 gene, which encodes a cytoskeletal protein. These genetic disorders result in a lack of functional muscle tissue and respiratory failure unless special treatment is taken. With such symptoms, Wright's syndrome can be diagnosed. Treatment for this disease is aimed at preventing the patient's chest from becoming completely immobile and ensuring maximum breathing capacity. The use of oxygen tanks, surgical chest reinforcement using special metal structures or implantable pumps can help some patients maintain sufficient lung function to survive. During the entire period of treatment, a patient with Wright's syndrome needs constant monitoring by a specialist who can help maintain vital body functions. This syndrome is a rare and life-threatening condition that can only be helped by starting treatment as early as possible.