Roberts Syndrome: Rare Genetic Impacts on Development
Roberts Syndrome Core Definition and Clinical Presentation Roberts Syndrome (RS), often referred to historically as the Pseudothalidomide Syndrome due to its striking phenotypic similarity to the effects of thalidomide exposure, is an extremely rare and severe autosomal recessive genetic disorder. It is fundamentally characterized by profound prenatal growth retardation and distinctive symmetrical limb reduction defects, […]