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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...
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| Formaat: | Artigo |
| Taal: | Inglês |
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Russian Ilizarov Scientific Center for Restorative Traumatology and Orthopaedics
2022-04-01
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| Reeks: | Гений oртопедии |
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