©The Author(s) 2023.
World J Orthop. Jan 18, 2023; 14(1): 13-22
Published online Jan 18, 2023. doi: 10.5312/wjo.v14.i1.13
Published online Jan 18, 2023. doi: 10.5312/wjo.v14.i1.13
Table 2 Mutated genes isolated in syndromic polydactyly
| Syndrome | Mutated gene(s) |
| Bardet-Biedl | CCDC28B, ARL6, MKS1, BBS8, SDCCAG8, LZTFL1, WDPCP, BBS4, BBS12, TMEM67, BBS1, BBS2, BBS6, BBS10, BBS9, BBS7, BBS5, CEP290, TRIM32, BBIP1, ALMS1, MKKS |
| McKusick-Kaufman | MKKS |
| Carpenter | P4HB, RAB23 |
| Saethre-Chotzen | TWIST1, FGFR2 |
| Poland syndrome | - |
| Greig cephalopolysyndactyly | GLI3 |
| Short-rib polydactyly | ATD1, LBN, DYNC2H1, IFT81 |
| Pallister-Hall | GLI3 |
| Triphalangeal thumb-polydactyly | LMBR1 |
| Smith-Lemli-Opitz | DHCR7 |
- Citation: Kyriazis Z, Kollia P, Grivea I, Stefanou N, Sotiriou S, Dailiana ZH. Polydactyly: Clinical and molecular manifestations. World J Orthop 2023; 14(1): 13-22
- URL: https://www.wjgnet.com/2218-5836/full/v14/i1/13.htm
- DOI: https://dx.doi.org/10.5312/wjo.v14.i1.13