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Retinoblastoma

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Description

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors.

GeneReviews

  • Mode of Inheritance

  • Autosomal dominant inheritance
  • Somatic mutation
  • Sporadic

VARIANTS

830

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Genes

External Links

  • OMIM

    180200

  • Orphanet

    790

  • HPO

    6425

  • Medgen

    C0035335

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