Epidemiology of congenital polydactyly and syndactyly in Hunan Province, China.
Zhou X, Li T, Kuang H, Zhou Y, Xie D, He J, Xiao J, Chen C, Jiang Y, Fang J, Wang H.
BMC Pregnancy Childbirth. 2024 Mar 23;24(1):216. doi: 10.1186/s12884-024-06417-y.
Ankyloglossia, Syndactyly and Polydactyly in the Pediatric Patient.
Morgado Dias J, Baptista A, Alegrete N, Areias C, Soares H.
Cureus. 2023 Feb 25;15(2):e35443. doi: 10.7759/cureus.35443. eCollection 2023 Feb.
Genetic Overview of Syndactyly and Polydactyly.
Ahmed H, Akbari H, Emami A, Akbari MR.
Plast Reconstr Surg Glob Open. 2017 Nov 2;5(11):e1549. doi: 10.1097/GOX.0000000000001549. eCollection 2017 Nov.
Surgical treatment of polydactyly and syndactyly during the 4th century AD.
Papadakis M, Manios A, Trompoukis C.
Acta Chir Belg. 2019 Feb;119(1):64-65. doi: 10.1080/00015458.2018.1534392. Epub 2018 Nov 2.
[Polydactyly and syndactyly as the most common congenital disorders of the limbs].
Gawlikowska-Sroka A.
Ann Acad Med Stetin. 2008;54(3):130-3.
Assessing the Readability of Online English and Spanish Resources for Polydactyly and Syndactyly.
Shin A, Paidisetty PS, Chivukula S, Wang LK, Chen W.
Ann Plast Surg. 2024 Nov 1;93(5):546-550. doi: 10.1097/SAP.0000000000004121.
Complex radial polydactyly in a Chinese family: inclusion of triphalangism, triplication, and syndactyly.
Xu J, Chen X, Teng X, Wang X, Chen H.
Ann Transl Med. 2021 Aug;9(16):1296. doi: 10.21037/atm-21-2773.
Two nonsense GLI3 variants are associated with polydactyly and syndactyly in two families by affecting the sonic hedgehog signaling pathway.
Shen X, Zhang S, Zhang X, Zhou T, Rui Y.
Mol Genet Genomic Med. 2022 Apr;10(4):e1895. doi: 10.1002/mgg3.1895. Epub 2022 Feb 26.
Uncovering a Diagnosis Through Reanalysis of UBA2 Variants in a Patient with Syndactyly, Polydactyly, and Aplasia Cutis Congenita: A Short Report and a Review of the Literature.
Liaqat K, Felipe K, Treat K, McPheron M, Weaver DD, Vetrini F, Conboy E.
Genet Test Mol Biomarkers. 2025 Apr;29(4):120-128. doi: 10.1089/gtmb.2025.0042.
Polydactyly and syndactyly linked to GLI3 and TBX5 mutations: A pediatric case report.
Leonardi R, Pellino G, Floridia E, Lo Bianco M, Ruggieri M, Cho SY, Pavone V, Pavone P, Polizzi A.
Glob Med Genet. 2024 Nov 30;12(1):100033. doi: 10.1016/j.gmg.2024.100033. eCollection 2025 Mar.
