Internal frontal hypobrosis syndrome is a rare disorder that occurs due to the growth and hardening of connective tissue in the area of the internal frontal thickening. This condition is characterized by constant pain and a feeling of heaviness in the forehead, bridge of the nose and upper eyelids. The syndrome can affect a person's quality of life and reduce their ability to perform daily tasks.
The causes of internal frontal hypoplasia syndrome are still unknown. However, some scientists associate its development with heredity and genetic factors. Other studies indicate a possible connection between this condition and a dysfunction of the immune system and excessive growth of connective tissue cells.
Clinical manifestations of internal frontal hiprobosis syndrome may include pain, swelling and redness of the frontal bone area, nosebleeds, decreased visual acuity, and even loss of consciousness. Often patients with internal frontal hilbrosis syndrome complain of morning headaches, which worsen with physical activity.
Treatment for internal frontal syndrome