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Article

[Neurofibromatosis: the most frequent hereditary tumor predisposition syndrome].

Wiener medizinische Wochenschrift (1946) - 1 Jun 2005

Wimmer Katharina

Abstract excerpt

With an incidence of one in 3000 to 4000 individuals, neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant genetic diseases and very likely the most frequent disorder with increased cancer risk. Approximately fifty percent of all patients are familial cases and the remaining half consists of sporadic cases with no affected parent. The hallmark clinical features present in over 90% of all...

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Source

Identifiers

PMID: 16035388
DOI: 10.1007/s10354-005-0185-1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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