Cutaneous Manifestations not Considered Diagnostic Criteria for Neurofibromatosis Type 1. A Case–Control Study

Cutaneous Manifestations not Considered Diagnostic Criteria for Neurofibromatosis Type 1. A Case–Control Study

[Display omitted] The diagnosis of Neurofibromatosis type 1 (NF1) is usually delayed in children without a family history. We aimed to define the prevalence and characteristics of prevalent skin manifestations in NF1 compared to the general population, which continue to be excluded from the diagnost...

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Veröffentlicht in:Actas dermo-sifiliográficas 2022-11, Vol.113 (10), p.923-929
Hauptverfasser: García-Martínez, F.J., Duat-Rodríguez, A., Andrés Esteban, E., Torrelo, A., Noguera Morel, L., Hernández-Martín, A.
Format: Artikel
Sprache:eng
Schlagworte:
Café-au-lait macules
fototipo
Juvenile xanthogranuloma
Máculas café con leche
Neurofibromatosis 1
Neurofibromatosis tipo 1
Nevus anemicus
Phototype
Prurito
Pruritus
Xantogranuloma juvenil
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Zusammenfassung:[Display omitted] The diagnosis of Neurofibromatosis type 1 (NF1) is usually delayed in children without a family history. We aimed to define the prevalence and characteristics of prevalent skin manifestations in NF1 compared to the general population, which continue to be excluded from the diagnostic criteria for NF1. Case–control study, matched by age groups, in which 108 patients with a diagnosis of NF1 and 137 healthy controls were included. The prevalence of nevus anemicus (NA) (p
ISSN:0001-7310
2173-5778
DOI:10.1016/j.ad.2022.05.014