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How I approach hereditary cancer predisposition in a child with cancer.
Kuhlen, Michaela; Wieczorek, Dagmar; Siebert, Reiner; Frühwald, Michael C.
  • Kuhlen M; University Children's Hospital Augsburg, Swabian Children's Cancer Center, Augsburg, Germany.
  • Wieczorek D; Institute of Human Genetics, Medical Faculty, Heinrich-Heine-University, Duesseldorf, Germany.
  • Siebert R; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.
  • Frühwald MC; University Children's Hospital Augsburg, Swabian Children's Cancer Center, Augsburg, Germany.
Pediatr Blood Cancer ; 66(11): e27916, 2019 11.
Article en En | MEDLINE | ID: mdl-31342632
ABSTRACT
Approximately 10% of all children with cancer are affected by a monogenic cancer predisposition syndrome. This has important implications for both the child and her/his family. The assessment of hereditary cancer predisposition is a challenging task for clinicians and genetic counselors in daily routine. It includes consideration of tumor genetics, specific features of the patient, and the medical/family history. To keep up with the pace of this rapidly evolving and increasingly complex field of genetic susceptibility, we suggest a systematic approach for the evaluation of the child with cancer and her/his family by an interdisciplinary team specialized in hereditary cancer predisposition.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndromes Neoplásicos Hereditarios / Asesoramiento Genético Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndromes Neoplásicos Hereditarios / Asesoramiento Genético Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Año: 2019 Tipo del documento: Article