Skeletal anomalies in patients with neurofibromatosis type 1
Introduction Neurofibromatosis type 1 (NF1) is one of the most common hereditary tumor syndromes. The average incidence of NF1 in the world is 1:3000 of the population. The characteristic signs of the disease are neurofibromas and café-au-lait macules on the skin. 60 % of patients with NF1 develop...
Main Author: | Rustam N. Mustafin |
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Format: | Article |
Language: | English |
Published: |
Russian Ilizarov Scientific Center for Restorative Traumatology and Orthopaedics
2022-04-01
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Series: | Гений oртопедии |
Subjects: |
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