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We are presenting a case of Adams Oliver Syndrome (AOS) in a newborn. This is rare congenital condition which presents with aplasia cutis congenita with transverse terminal limb defects with or without neurological manifestations. Diagnosis is based on clinical examination. Genetic diagnosis is available .Once the AOS-related pathogenic variants have been identified in an affected family member, molecular genetic prenatal testing for a pregnancy at increased risk and preimplantation geneticdoi:10.18535/jmscr/v5i4.109 fatcat:r6bwwqviingdvnbpyjzitqbrjm