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Juvenile xanthogranuloma: A possible diagnostic criterion for Neurofibromatosis type 1 in young children.
Calligaris, Lorenzo; Cortellazzo Wiel, Luisa; Sartor, Emma; Berti, Irene; Bruno, Irene; Barbi, Egidio; Magnolato, Andrea.
Afiliación
  • Calligaris L; Institute for Maternal and Child Health-IRCCS Burlo Garofolo, Trieste, Italy.
  • Cortellazzo Wiel L; Department of Medicine, Surgery and Health Sciences, University of Trieste, Trieste, Italy.
  • Sartor E; Department of Medicine, Surgery and Health Sciences, University of Trieste, Trieste, Italy.
  • Berti I; Institute for Maternal and Child Health-IRCCS Burlo Garofolo, Trieste, Italy.
  • Bruno I; Institute for Maternal and Child Health-IRCCS Burlo Garofolo, Trieste, Italy.
  • Barbi E; Institute for Maternal and Child Health-IRCCS Burlo Garofolo, Trieste, Italy.
  • Magnolato A; Department of Medicine, Surgery and Health Sciences, University of Trieste, Trieste, Italy.
Am J Med Genet A ; 185(12): 3895-3896, 2021 12.
Article en En | MEDLINE | ID: mdl-34250743
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neurofibromatosis 1 / Xantogranuloma Juvenil / Predisposición Genética a la Enfermedad Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Italia
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neurofibromatosis 1 / Xantogranuloma Juvenil / Predisposición Genética a la Enfermedad Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Italia