Subglottic neurofibromatosis should be considered in cases of respiratory distress in children who do not respond to medical treatment. Early diagnosis and surgical treatment can help resolve the obstruction of the child's larynx, helping the child return to normal activities soon.

Subglottic neurofibroma is an extremely rare disease. In our country, there have been a number of reported cases. The symptoms are nonspecific and can be easily confused with other tumors around the neck.

Neurofibromatosis type 2 is a genetic neurofibromatosis caused by a disorder of chromosome 22. Although benign, the tumor can affect hearing or cause balance problems.

Neurofibromatosis type 1 is a dominant genetic disease caused by a chromosome disorder. Most of the time, the disease does not seriously affect health, but when the tumor grows large, causing scoliosis, vision loss, etc., it can be treated with surgery or radiation therapy.