1 results match your criteria: "France4Centre de Compétence Maladies Rares Neurofibromatose 1[Affiliation]"
Juvenile xanthogranuloma and nevus anemicus in the diagnosis of neurofibromatosis type 1.
JAMA Dermatol
January 2014
Dermatology, Centre Hospitalier Universitaire de Dijon3Research Unit EA 4271 Génétique des Anomalies du Développement, Université de Bourgogne, PRES Bourgogne-Franche Comté, France4Centre de Compétence Maladies Rares Neurofibromatose 1, Dijon, France.
Importance: The diagnosis of neurofibromatosis type 1 (NF1) is based on 7 clinical criteria. However, they are of limited value before the age of 2 years. Juvenile xanthogranuloma (JXG) and nevus anemicus (NA) are commonly observed in children with NF1 and may be useful diagnostic clues.
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