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- W2090903089 abstract "Neurofibromatosis type 1 genetic disorder is an inherited autosomal dominant trait with variable penetrance and expressivity and occurs in one of every 2000–3300 live births. Neurofibromatosis type 2, on the other hand, afflicts only one in approximately 50 000 people. Within these patients, the frequency of intra-oral involvement of neurofibromas has been reported in a range of 4–7%. Alternatively, neurofibromas in the oral cavity minus the presence of a neurofibromatosis disease has been documented but the prevalence is even less than stated earlier making a solitary neurofibroma of the tongue a rare occurrence. This article reports an unusual presentation of a neurofibroma masquerading as a lipoma with the tumour occurring at the base of the tongue." @default.
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- W2090903089 date "2010-04-01" @default.
- W2090903089 modified "2023-09-26" @default.
- W2090903089 title "Unusual presentation of a hypoglossal nerve neurofibroma" @default.
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- W2090903089 doi "https://doi.org/10.1111/j.1752-248x.2010.01058.x" @default.
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