Camptodactyly and DiGeorge syndrome: A rare hand anomaly

Parkman, 1998, DiGeorge syndrome: Still an enigma, J Pediatr, 132, 3, 10.1016/S0022-3476(98)70475-5 Fung, 2015, Practical guidelines for managing adults with 22q11.2 deletion syndrome, Genet Med, 17, 599, 10.1038/gim.2014.175 Wall, 2018, Camptodactyly treatment for the lesser digits, J Hand Surg Am, 43, 10.1016/j.jhsa.2018.03.023 Spyropoulou, 2016, Dupuytren in a Child: Rare presentation of a rare clinical entity, J Hand Surg Am, 41, e477, 10.1016/j.jhsa.2016.08.011 Ming, 1997, Skeletal anomalies and deformities in patients with deletions of 22q11, Am J Med Genet, 72, 210, 10.1002/(SICI)1096-8628(19971017)72:2<210::AID-AJMG16>3.0.CO;2-Q Noël, 2014, Fetal phenotype associated with the 22q11 deletion, Am J Med Genet A, 164A, 2724, 10.1002/ajmg.a.36720 Couser, 2017, Camptodactyly and the 22q11.2 deletion syndrome, Am J Med Genet A, 173, 515, 10.1002/ajmg.a.38029 Oskarsdóttir, 2005, Presenting phenotype in 100 children with the 22q11 deletion syndrome, Eur J Pediatr, 164, 146, 10.1007/s00431-004-1577-8 Swartz, 2008, MOC-PS(SM) CME article: Dupuytren's disease, Plast Reconstr Surg, 121, 1, 10.1097/01.prs.0000305932.46121.84 Rhomberg, 2002, Dupuytren's disease in children-differential diagnosis, J Pediatr Surg, 37, E7, 10.1053/jpsu.2002.31646