Table 1.
Syndrome | % of OS | Genes Mutated | References |
---|---|---|---|
Li–Fraumeni syndrome | 12% | TP53 | [20,28] |
Retinoblastoma syndrome | 7% | RB | [49] |
Rothmund–Thomson type II (RTS II) syndrome | 32% | RECQL4 | [28] |
RAPALIDINO syndromes | 13.3% | RECQL4 | [20] |
Werner syndrome | WRN | ||
Bloom syndrome | BLM | ||
Diamond–Blackfan anemia | 5.4% 0.9% |
RPS19, RPL5, RPL11, RPL35A,
RPS24, RPS17, RPS7, RPS10, RPS26 |
[47] [48] |