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Archives of Disease in Childhood 1999;80:1-3; doi:10.1136/adc.80.1.1
Copyright © 1999 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.
Arch Dis Child 1999;80:1-3 ( January )

Annotation

Genes and cancer

The first 150 words of the full text of this article appear below.

    Introduction

In developed countries, approximately 1 in 600 children develop cancer before they are 15 years old. Half of all childhood malignancies are diagnosed during the first 5 years of life. About 33% of cases are leukaemias, 25% brain tumours, and 10-12% lymphomas. The remaining cases are mainly embryonal tumours including neuroblastoma, Wilms's tumour, embryonal rhabdomyosarcoma, retinoblastoma, and hepatoblastoma.1 2 Many of the leukaemias and brain tumours also constitute embryonal neoplasms. The histological appearance of embryonal neoplasms resembles that seen in the developing embryo and fetus. The early onset of these neoplasms and their embryonal appearance strongly suggest that prenatal, including genetic, factors are important. This article considers the role of genetic predisposition in the development of childhood cancer.

Genetic predisposition to cancer may be considered under four areas:

  • highly penetrant genes that give rise to distinct familial clusters of cancers with a clear pattern of inheritance

  • genes that confer a lower penetrance, with most gene . . . [Full text of this article]


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