Hypopigmented macules in neurofibromatosis type 1: A case control study - 10/03/21
Doi : 10.1016/j.jaad.2020.06.071
Francisco Javier García-Martínez, MD, PhD a, ⁎ 
, Anna Duat-Rodriguez, MD, PhD b, Antonio Torrelo, MD, PhD c, Lucero Noguera-Morel, MD c, Angela Hernández-Martín, MD, PhD c
, Anna Duat-Rodriguez, MD, PhD b, Antonio Torrelo, MD, PhD c, Lucero Noguera-Morel, MD c, Angela Hernández-Martín, MD, PhD c a Dermatology Department, Clínica Universidad de Navarra, Madrid, Spain
b Pediatric Neurology Department, Hospital Infantil Universitario Niño Jesús, Madrid, Spain
c Dermatology Department, Hospital Infantil Universitario Niño Jesús, Madrid, Spain
∗Reprint requests: Francisco Javier García-Martínez, MD, PhD, C/ Marquesado de Santa Marta 1, 28027, Madrid, SpainC/ Marquesado de Santa Marta 1Madrid28027Spain
| Funding sources: None. |
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| Conflicts of interest: None disclosed. |
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| This study is included in the doctoral thesis entitled “Clinical and ultrasonographic study of the neurofibromatosis type 1 in a pediatric population” (irGestionarConsulta.do). This study was also presented at the 75th American Academy of Dermatology Annual Meeting, Orlando, FL, March 3-7, 2017, as an e-poster under the title “Hypopigmented Macules: A Common Finding in Neurofibromatosis Type 1.” |
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| IRB approval status: Reviewed and approved by Niño Jesús Hospital Ethics and Clinical Research Committee (R-0055/14 Acta no. 09/14, October 28, 2014). |
© 2020
American Academy of Dermatology, Inc.. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 84 - N° 4
P. 1128-1130 - avril 2021 Retour au numéro
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