Neurofibromatosis is an autosomal dominant disease, the probability of inheritance is about 50%, and some other part is related to gene mutation, so there is a certain probability of inheritance.
Neurofibromatosis is a disease that involves multiple systems, and common clinical manifestations include milky coffee-colored macules on the skin, gliomas on the optic nerve, and symptoms of tumor compression.
The treatment of neurofibromatosis is based on symptomatic and surgical treatment, through which the patient’s symptoms can be alleviated, the recurrence of the tumor can be reduced, and the quality of life can be improved. Timely review is also needed to prevent tumor recurrence.
Due to the high heritability of neurofibromatosis, it is recommended that people with a family history of neurofibromatosis should have regular checkups and prenatal tests, and once diagnosed, they need to receive standardized treatment under the guidance of doctors.