A case of neurofibromatosis type 1 with neurofibromatosis type 1-related and neurofibromatosis type 1-unrelated tumors: a case report

Abstract Background Neurofibromatosis type 1 is an autosomal dominantly inherited disorder caused by pathogenic variants in the neurofibromatosis type 1 gene, resulting in a predisposition to multiple tumors. Typical neurofibromatosis type 1-associated tumors include cutaneous and plexiform neurofib...

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Hlavní autoři:	Tabea I. Hartung, Qais Karimi, Lan Kluwe, Said C. Farschtschi
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	BMC 2025-10-01
Edice:	Journal of Medical Case Reports
Témata:	Neurofibromatosis type 1 NF1 Rare tumor spectrum NF1-unrelated tumors
On-line přístup:	https://doi.org/10.1186/s13256-025-05599-z
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