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- W2019012365 abstract "PURPOSE: Neurofibromatosis (NF) is one of the diseases of the phacomatosis family. The incidence of the common subtype NF1 ranges between 1:2'300–1:3'000. About half of the cases are familial with an autosomal dominant inheritance, the rest are due to spontaneous mutations. Consequences are dyplasia of ecto- and mesoderm. Diagnostic criteria are café-au-lait maculas, neurofibromas, etc. Although thoracic manifestations are diverse and quite common, the involvement of lung parenchyma in NF1 appears to be rare." @default.
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- W2019012365 date "2009-10-01" @default.
- W2019012365 modified "2023-09-25" @default.
- W2019012365 title "PULMONARY INVOLVEMENT IN NEUROFIBROMATOSIS (VON RECKLINGHAUSEN'S DISEASE): AN UNCOMMON MANIFESTATION" @default.
- W2019012365 doi "https://doi.org/10.1378/chest.136.4_meetingabstracts.116s-b" @default.
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