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pubmed-article:9881680pubmed:abstractTextWe describe a girl with a brain-stem tumour and symptoms very similar to those of Rett syndrome (RS). Her early history was uneventful and development was normal (except for hypotonia). At the age of 6 months her development slowed. Subsequently, deterioration occurred and the features characteristic of RS were seen: loss of purposeful hand use, stereotypic hand movements, impaired social contact, decelerated head growth, and ataxia. Cerebral CT at the age of 3 years and 4 months revealed a tumour in the region of the pons and hydrocephalus. We suggest that a pons/midbrain tumour appearing at an early age may affect the developing CNS and cause symptoms similar to those of RS. A possible causal connection between midbrain pathology and RS is supported by this case.lld:pubmed
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pubmed-article:9881680pubmed:authorpubmed-author:PaetauAAlld:pubmed
pubmed-article:9881680pubmed:authorpubmed-author:RiikonenRRlld:pubmed
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pubmed-article:9881680pubmed:dateRevised2009-11-11lld:pubmed
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pubmed-article:9881680pubmed:year1998lld:pubmed
pubmed-article:9881680pubmed:articleTitlePons tumour behind a phenotypic Rett syndrome presentation.lld:pubmed
pubmed-article:9881680pubmed:affiliationHospital for Children and Adolescents, Helsinki, Finland.lld:pubmed
pubmed-article:9881680pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9881680pubmed:publicationTypeCase Reportslld:pubmed
pubmed-article:9881680pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed