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A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.
Scollon, Sarah; Anglin, Amanda Knoth; Thomas, Martha; Turner, Joyce T; Wolfe Schneider, Kami.
Afiliação
  • Scollon S; Department of Pediatrics, Baylor College of Medicine, Texas Children's Cancer Center, Texas Children's Hospital, 1102 Bates St, FC 1200, Houston, TX, 77030, USA. sxscollo@txch.org.
  • Anglin AK; Myriad Genetic Laboratories, Dayton, OH, USA.
  • Thomas M; University of Virginia, Charlottesville, VA, USA.
  • Turner JT; Department of Genetics and Metabolism, Children's National Medical Center, Washington, DC, USA.
  • Wolfe Schneider K; Department of Pediatrics, University of Colorado, Center for Cancer and Blood Disorders, Children's Hospital Colorado, Aurora, CO, USA.
J Genet Couns ; 26(3): 387-434, 2017 Jun.
Article em En | MEDLINE | ID: mdl-28357779
ABSTRACT
An understanding of the role of inherited cancer predisposition syndromes in pediatric tumor diagnoses continues to develop as more information is learned through the application of genomic technology. Identifying patients and their relatives at an increased risk for developing cancer is an important step in the care of this patient population. The purpose of this review is to highlight various tumor types that arise in the pediatric population and the cancer predisposition syndromes associated with those tumors. The review serves as a guide for recognizing genes and conditions to consider when a pediatric cancer referral presents to the genetics clinic.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Predisposição Genética para Doença Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Genet Couns Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Predisposição Genética para Doença Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Genet Couns Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos