Abstract
Skeletal pathology as a manifestation of type I neurofibromatosis is relatively rare in 1520% of patients, and each case of neurofibromatosis bears the stamp of individual uniqueness [1, 2]. Among the indications of the involvement of bone structures in the destructive process, we did not find a description of a pathological fracture of the acetabulum and methods for restoring the support ability of the pelvis and hip in this disease.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have