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Rett syndrome (RTT) is a rare neuro-developmental disorder (incidence: approximately one out of 10,000 female births) that reached worldwide prominence in the early 1980s. Owing to its predominance in females, Rett syndrome is regarded as a genetic disorder. Over the past 25 years, understanding of the clinical features and natural history of this unique neuro-developmental disorder has evolved dramatically. Significant advances have emerged in recent years regarding our understanding of the clinical features, molecular genetics
Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry’s standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book. It has survived not only five centuries, but also the leap into electronic typesetting, remaining essentially unchanged. It was popularised in the 1960s with the release of Letraset sheets containing Lorem Ipsum
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