Congenital, Hereditary, and Neonatal Diseases and Abnormalities: News and Research on Neurofibromatosis 1

MeSH tree: C16.320.400.560.400

Earlier detection of a malignancy in neurofibromatosis type 1

Neurofibromatosis type 1 (NF1) is a common genetic condition, affecting 1 in 3,000 individuals, and people with NF1 are at greater risk of developing a rare, aggressive form of cancer. Diagnosing malignant peripheral nerve ...

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