Clinical and biological progress over 50 years in Rett syndrome

Leonard, H., Cobb, S. and Downs, J. (2017) Clinical and biological progress over 50 years in Rett syndrome. Nature Reviews Neurology, 13(1), pp. 37-51. (doi: 10.1038/nrneurol.2016.186) (PMID:27934853)

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Abstract

In the 50 years since Andreas Rett first described the syndrome that came to bear his name, and is now known to be caused by a mutation in the methyl-CpG-binding protein 2 (MECP2) gene, a compelling blend of astute clinical observations and clinical and laboratory research has substantially enhanced our understanding of this rare disorder. Here, we document the contributions of the early pioneers in Rett syndrome (RTT) research, and describe the evolution of knowledge in terms of diagnostic criteria, clinical variation, and the interplay with other Rett-related disorders. We provide a synthesis of what is known about the neurobiology of MeCP2, considering the lessons learned from both cell and animal models, and how they might inform future clinical trials. With a focus on the core criteria, we examine the relationships between genotype and clinical severity. We review current knowledge about the many comorbidities that occur in RTT, and how genotype may modify their presentation. We also acknowledge the important drivers that are accelerating this research programme, including the roles of research infrastructure, international collaboration and advocacy groups. Finally, we highlight the major milestones since 1966, and what they mean for the day-to-day lives of individuals with RTT and their families.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Cobb, Dr Stuart
Authors: Leonard, H., Cobb, S., and Downs, J.
College/School:College of Medical Veterinary and Life Sciences > School of Psychology & Neuroscience
Journal Name:Nature Reviews Neurology
Publisher:Nature Publishing Group
ISSN:1759-4758
ISSN (Online):1759-4766
Published Online:09 December 2016
Copyright Holders:Copyright © 2016 Nature Publishing Group
First Published:First published in Nature Reviews Neurology 13(1):37-51
Publisher Policy:Reproduced in accordance with the copyright policy of the publisher

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