Rett syndrome Síndrome de Rett

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dc.contributor.authorSalomao Schwartzman J.
dc.date.accessioned2024-03-13T01:46:07Z
dc.date.available2024-03-13T01:46:07Z
dc.date.issued2003
dc.description.abstractThis article is focus on the currently knowledge about Rett syndrome, based on the more recent information in the international literature on genetic and epidemiological aspects of this condition, as well as on its clinical and laboratory diagnosis, neuropathology, electrophysiology, and clinical outcome (epilepsy, respiratory disorders, autonomic disturbances and nutritional aspects). Although it has been known as a female condition, nowadays it is described the possibility of affected males with a different phenotype.
dc.description.firstpage110
dc.description.issuenumber2
dc.description.lastpage113
dc.description.volume25
dc.identifier.doi10.1590/s1516-44462003000200012
dc.identifier.issn1516-4446
dc.identifier.urihttps://dspace.mackenzie.br/handle/10899/37991
dc.relation.ispartofRevista Brasileira de Psiquiatria
dc.rightsAcesso Aberto
dc.subject.otherlanguageClinical genetics
dc.subject.otherlanguageEpilepsy
dc.subject.otherlanguageMental retardation
dc.subject.otherlanguageMultiple handicap
dc.subject.otherlanguageRett syndrome
dc.titleRett syndrome Síndrome de Rett
dc.typeArtigo de revisão
local.scopus.citations11
local.scopus.eid2-s2.0-0043163388
local.scopus.updated2024-05-01
local.scopus.urlhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0043163388&origin=inward
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