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Stereotypies in Rett syndrome: Analysis of 83 patients with and without detected MECP2 mutations

✍ Scribed by Temudo, T.; Oliveira, P.; Santos, M.; Dias, K.; Vieira, J.; Moreira, A.; Calado, E.; Carrilho, I.; Oliveira, G.; Levy, A.; Barbot, C.; Fonseca, M.; Cabral, A.; Dias, A.; Cabral, P.; Monteiro, J.; Borges, L.; Gomes, R.; Barbosa, C.; Mira, G.; Eusebio, F.; Santos, M.; Sequeiros, J.; Maciel, P.


Book ID
118150259
Publisher
Lippincott Williams and Wilkins
Year
2007
Tongue
English
Weight
523 KB
Volume
68
Category
Article
ISSN
0028-3878

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Movement disorders in Rett syndrome: An
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## Abstract Rett syndrome (RS) is one of the best human models to study movement disorders. Patients evolve from a hyperkinetic to a hypokinetic state, and a large series of abnormal movements may be observed along their lives such as stereotypies, tremor, chorea, myoclonus, ataxia, dystonia, and r