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In this report, a 32 years old woman with increased nuchal translucency at 11th weeks of gestation and the diagnosis of Arthrogryposis Multiplex Congenita is demonstrated. After informing the family, chorion villus sampling (CVS) was performed. Fetal chromosomal analysis was reported as normal (XX). On control, lower and upper extremities had flexion contractures in 2D obstetrical ultrasonographic examination, besides bilateral club foot and absence of movement was detected. The family wasdoaj:c91e4cb38b56490283ff1073221f32a1 fatcat:6pb2c6ickfbkbpp2k5i7y7liru