[Translated article] Neurofibromatosis Type 1: Diagnostic Timelines in Children
Background and objectives: Diagnosis of neurofibromatosis 1 (NF1) diagnosis is challenging in young children without a family history of NF1. The aims of this study were to estimate diagnostic delays in children without a family history of NF1 and to examine the effects of considering café-au-lait m...
Main Authors: | F.J. García-Martínez, A. Hernández-Martín |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2023-03-01
|
Series: | Actas Dermo-Sifiliográficas |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S0001731023000728 |
Similar Items
-
Cutaneous Manifestations not Considered Diagnostic Criteria for Neurofibromatosis Type 1. A Case–Control Study
by: F.J. García-Martínez, et al.
Published: (2022-11-01) -
Unroofed coronary sinus in a patient with neurofibromatosis type 1
by: Luciano Pereira Bender, et al.
Published: (2013-12-01) -
Xantogranuloma Juvenil Cutâneo Disseminado: Relato de Caso
by: Débora Bacellar Cruz Nunes, et al.
Published: (2019-03-01) -
Neuroibromatosis tipo l: relación genotipo-fenotipo
by: Mariana Teresa Gómez-López, et al.
Published: (2020-01-01) -
Juvenile Xantogranuloma: clinical case presentation and a review of the literature
by: Ricardo Flaminio Rojas López, et al.
Published: (2003-12-01)