Neurofibromatosis 1 French national guidelines based on an extensive literature review since 1966

Neurofibromatosis 1 French national guidelines based on an extensive literature review since 1966

Abstract Neurofibromatosis type 1 is a relatively common genetic disease, with a prevalence ranging between 1/3000 and 1/6000 people worldwide. The disease affects multiple systems with cutaneous, neurologic, and orthopedic as major manifestations which lead to significant morbidity or mortality. In...

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Bibliographic Details
Main Authors: Christina Bergqvist, Amandine Servy, Laurence Valeyrie-Allanore, Salah Ferkal, Patrick Combemale, Pierre Wolkenstein, NF France Network
Format: Article
Language:English
Published: BMC 2020-02-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Neurofibromatosis type 1
Guidelines
Management
Multidisciplinary
Diagnosis
Genetic counseling
Online Access:https://doi.org/10.1186/s13023-020-1310-3

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