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Neurofibromatosis tipo 1 (NF1): [revisión] / Neurofibromatosis type 1 (NF1): [review]
Gaviria Villa, Claudia; Larralde, Margarita.
  • Gaviria Villa, Claudia; Hospital Ramos Mejía. Sector de Dermatología Pediátrica. Buenos Aires. AR
  • Larralde, Margarita; Hospital Alemán. Servicio de Dermatología. Buenos Aires. AR
Dermatol. pediatr. latinoam. (Impr.) ; 7(1): 7-13, ene.-abr. 2009. ilus
Article in Spanish | LILACS | ID: lil-598141
RESUMEN
La neurofibromatosis tipo 1 es la genodermatosis más común, heredada de manera autosómica dominante. Presenta una distribución mundial y no tiene predominio racial. Afecta fundamentalmente la piel, los ojos y los sistemas nervioso y esquelético. El presente trabajo consiste en una revisión sobre su patogénesis, manifestaciones clínicas, criterios diagnósticos, tratamiento y pronóstico.
ABSTRACT
Neurofibromatosis type 1 is the most common genodermatosis, inherited in an autosomal dominant way. It has a worldwide distribution and has no racial predilection. Skin, eyes, nervous system and bones are usually affected. The present work reviews its pathogenesis, clinical manifestations, diagnostic criteria, treatment and prognoses.
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Index: LILACS (Americas) Main subject: Neurofibromatosis 1 Type of study: Prognostic study Limits: Child, preschool / Humans / Infant Language: Spanish Journal: Dermatol. pediatr. latinoam. (Impr.) Journal subject: Dermatology / Pediatrics Year: 2009 Type: Article Affiliation country: Argentina Institution/Affiliation country: Hospital Alemán/AR / Hospital Ramos Mejía/AR

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Index: LILACS (Americas) Main subject: Neurofibromatosis 1 Type of study: Prognostic study Limits: Child, preschool / Humans / Infant Language: Spanish Journal: Dermatol. pediatr. latinoam. (Impr.) Journal subject: Dermatology / Pediatrics Year: 2009 Type: Article Affiliation country: Argentina Institution/Affiliation country: Hospital Alemán/AR / Hospital Ramos Mejía/AR