| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3084277 | Pediatric Neurology | 2016 | 7 Pages |
Abstract
A significant portion of the patients presenting with isolated café-au-lait macules at initial consultation might not have NF1. Genetic testing could help guide the follow-up of those patients, but further evidence is required to make recommendations.
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Authors
Anne MD, MSc, Albert MD, Sebastien MD, MSc,