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Article

[Neurofibromatosis type 1 or Von Recklinghausen's disease].

La Revue de medecine interne - 1 Mar 2005

Pinson S, Wolkenstein P

Abstract excerpt

OBJECTIVES: Neurofibromatosis 1(NF1) is one of the most common genetic diseases. NF1 is an autosomal dominant genetic disorder and half of affected individuals have NF1 as the result of a new gene NF1 mutation. The offspring of an affected individual have a 50% risk of inheriting the altered NF1 gene. The disease manifestations are extremely variable, even within a family. NF1 is characterized by multiple cafe au...

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Identifiers

PMID: 15777582
DOI: 10.1016/j.revmed.2004.06.011

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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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