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. 2014 Jan;50(1):1-3.
doi: 10.1016/j.pediatrneurol.2013.08.018. Epub 2013 Nov 5.

The American history of Rett syndrome

Alan Percy  1
Affiliations

The American history of Rett syndrome

Alan Percy. Pediatr Neurol. 2014 Jan.
No abstract available

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Conflict of interest statement

The author has no conflicts.

References

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    1. Rett A. Cerebral atrophy associated with hyperammonemia. In: Vinkin PJ, Bruyn GW, editors. Handbook of Clinical Neurology. Amsterdam: North Holland Publishing Company; 1977. pp. 305–329.
    1. Hagberg B, Aicardi J, Dias K, Ramos O. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett’s syndrome: report of 35 cases. Ann Neurol. 1983;14:471–479. - PubMed
    1. Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet. 1999;23:185–188. - PubMed
    1. Neul JL, Kaufmann WE, Glaze DG, et al. Rett syndrome: revised diagnostic criteria and nomenclature. Ann Neurol. 2010;68:944–950. - PMC - PubMed

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