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The neurofibromatoses. An overview
The Italian Journal of Neurological Sciences, 1999The last two decades have seen clinical and molecular delineation of the different forms of neurofibromatosis. Differentiation of these forms is not just an academic exercise: their natural history, management and genetic counselling are quite different.
RUGGIERI, MARTINO, HUSON SM
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2023
Abstract The neurofibromatoses include neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2), and schwannomatosis. These are genetically distinct tumor suppressor syndromes with increased incidence of central and peripheral nervous system tumors and an autosomal dominant inheritance pattern.
Kun-Wei Song, Scott R. Plotkin
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Abstract The neurofibromatoses include neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2), and schwannomatosis. These are genetically distinct tumor suppressor syndromes with increased incidence of central and peripheral nervous system tumors and an autosomal dominant inheritance pattern.
Kun-Wei Song, Scott R. Plotkin
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Der Radiologe, 2013
Neurofibromatosis type 1 (NF1) and type 2 (NF2) are hereditary autosomal dominant neurocutaneous disorders, the phacomatoses, characterized by the development of tumors derived from the cells of the peripheral nerve sheath and also includes schwannomatosis.
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Neurofibromatosis type 1 (NF1) and type 2 (NF2) are hereditary autosomal dominant neurocutaneous disorders, the phacomatoses, characterized by the development of tumors derived from the cells of the peripheral nerve sheath and also includes schwannomatosis.
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2005
Abstract Three clinically and genetically distinct diseases are classified as neurofibromatoses: neurofibromatosis 1 (NF1), neurofibromatosis 2 (NF2) and schwannomatosis. The inclusion of these three conditions in a single group reflects the fact that they share certain clinical features, but it is important to distinguish each disease ...
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Abstract Three clinically and genetically distinct diseases are classified as neurofibromatoses: neurofibromatosis 1 (NF1), neurofibromatosis 2 (NF2) and schwannomatosis. The inclusion of these three conditions in a single group reflects the fact that they share certain clinical features, but it is important to distinguish each disease ...
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