Sarman, HakanMemisoglu, KayaBaran, Tuncay2024-09-252024-09-2520131309-3878https://hdl.handle.net/20.500.12491/13444Larsen syndrome is a rare genetic disorder, with an incidence of 1/100,000. Joint hypermobility, congenital joint dislocations, spinal deformity and distinctive facial features are characteristic findings in the newborns. Congenital orthopedics pathology is rare with this syndrome. Herein we present a case with Larsen syndrome and discuss it with a brief review of the literature.trinfo:eu-repo/semantics/closedAccessCongenital Joint DislocationsLarsen SyndromeSpinal DeformityReview Article535154WOS:000420972400012N/A