François J
Mod Probl Ophthalmol. 1977;18:165-72.
Retinoblastoma may be due to (1) a somatic mutation, which is not hereditary, (2) a germinal mutation, which is dominantly inherited, and (3) a deletion of the long arm of chromosome 13. In unilateral cases of retinoblastoma, the risk for the offspring is 5-6%, as 10-15% of these cases are due to a germinal mutation. In all the bilateral cases and in the unilateral hereditary cases, the risk for the offspring or the sibs is 40-50% depending on the penetrance of the gene.
(1)体细胞突变,不具有遗传性;(2)生殖细胞突变,呈显性遗传;(3)13号染色体长臂缺失。在视网膜母细胞瘤单侧病例中,后代患病风险为5%-6%,因为这些病例中有10%-15%是由生殖细胞突变引起的。在所有双侧病例和单侧遗传性病例中,根据基因的外显率,后代或同胞的患病风险为40%-50%。