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临床试验/NL-OMON37736
NL-OMON37736尚未招募不适用

Comprehensive detection of childhood cancer predisposing genes using exome sequencing: The next step towards personalized treatment and cancer prevention. - Detection of childhood cancer predisposing genes using exome sequencing

niversitair Medisch Centrum Sint Radboud0 个研究点目标入组 180 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
180

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
2 至 99(—)

入选标准

  • Individuals diagnosed with any form of childhood cancer and one of the following characteristics will be included:
  • Intellectual disability,
  • Congenital anomalies,
  • Adult type of cancer in a child
  • First or second degree relative with the same type of cancer.
  • Second primary malignancy
  • as well as their parents

排除标准

  • A known genetic defect in the family for a cancer unrelated condition, of which the child might be a carrier but about which the child/parents do not want to be informed.

研究者

发起方
niversitair Medisch Centrum Sint Radboud

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