Diagnostic difficulties and possibilities of NF1-like syndromes in childhood.

Pinti, Eva; Nemeth, Krisztina; Staub, Krisztina; Lengyel, Anna; Fekete, Gyorgy; Haltrich, Iren

Pinti, Eva; Nemeth, Krisztina; Staub, Krisztina; Lengyel, Anna; Fekete, Gyorgy; Haltrich, Iren.

Afiliação

Pinti E; II. Department of Pediatrics, Semmelweis University, Tuzolto utca 7-9, Budapest, 1094, Hungary. pinti.eva@med.semmelweis-univ.hu.
Nemeth K; II. Department of Pediatrics, Semmelweis University, Tuzolto utca 7-9, Budapest, 1094, Hungary.
Staub K; II. Department of Pediatrics, Semmelweis University, Tuzolto utca 7-9, Budapest, 1094, Hungary.
Lengyel A; II. Department of Pediatrics, Semmelweis University, Tuzolto utca 7-9, Budapest, 1094, Hungary.
Fekete G; II. Department of Pediatrics, Semmelweis University, Tuzolto utca 7-9, Budapest, 1094, Hungary.
Haltrich I; II. Department of Pediatrics, Semmelweis University, Tuzolto utca 7-9, Budapest, 1094, Hungary.

BMC Pediatr ; 21(1): 331, 2021 07 29.

Article em En | MEDLINE | ID: mdl-34325699

Assuntos

Neurofibromatose 1; Manchas Café com Leite/genética; Criança; Testes Genéticos; Humanos; Neurofibromatose 1/diagnóstico; Neurofibromatose 1/genética; Fenótipo; Síndrome

Palavras-chave

Cafe-au-Lait spots; Child; Early diagnosis; Genes, tumor suppressor; National Institutes of Health (U.S.); Neurofibroma; Neurofibromatosis 1; Neurofibromatosis type 1-like syndrome; Oncogenes; Risk assessment; Tumor predisposition

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neurofibromatose 1 Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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