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Article

Identification of three clinical neurofibromatosis 1 subtypes: Latent class analysis of a series of 1351 patients.

Journal of the European Academy of Dermatology and Venereology : JEADV - 1 May 2022

Bergqvist C, Fertitta L, Ezzedine K, Jannic A, Zehou O, Ferkal S, Combemale P, Barbarot S, Mazereeuw-Hautier J, Sbidian E, Wolkenstein P

Abstract excerpt

BACKGROUND: Neurofibromatosis 1 (NF1) is one of the most common inherited disorders characterized by mutations in the tumour suppressor gene NF1. Its clinical manifestations are highly variable and unpredictable. A specific NF1 mutation does not predict the severity or complications of the disease. OBJECTIVE: The objective of this study was to build an empirical classification scheme without any a priori...

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Identifiers

PMID: 35098592
DOI: 10.1111/jdv.17974

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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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