Arthrogryposis Multiplex Congenita: Case Report Ayla AKTULAY, Saliha SAĞNIÇ, Özlem MORALOĞLU TEKİN, Yaprak ENGİN ÜSTÜN, Elif Gül YAPAR EYİ, Leyla MOLLAMAHMUTOĞLU Ankara, Turkey Arthrogryposis multiplex congenita (AMC), characterized by multiple congenital joint contractures due to decreased fetal movements, is a non-progressive rare syndrome. Prevalence is determined to be 1 in 3000 deliveries. Although it is autosomal recessively inherited, sporadic cases have also been reported. Prenatal diagnosis of AMC is difficult. Here we report a case with a diagnosis of AMC not diagnosed during antenatal follow-up. Key Words: Arthrogryposis, Multiplex, Congenita
Arthrogryposis Multiplex Congenita: Case Report Ayla AKTULAY, Saliha SAĞNIÇ, Özlem MORALOĞLU TEKİN, Yaprak ENGİN ÜSTÜN, Elif Gül YAPAR EYİ, Leyla MOLLAMAHMUTOĞLU Ankara, Turkey
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