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Primary Ciliary Dyskinesia and Hydrocephalus With Aqueductal Stenosis

dc.contributor.authorVieira, JP
dc.contributor.authorLopes, P
dc.contributor.authorSilva, R
dc.date.accessioned2014-03-25T11:12:47Z
dc.date.available2014-03-25T11:12:47Z
dc.date.issued2011
dc.description.abstractWe report 1 female patient with situs inversus, dextrocardia, a complex heart malformation, hydrocephalus due to aqueductal stenosis, and abnormal ultrastructure of the respiratory epithelium cilia. Several animal models of this disorder implicate abnormal ciliary function in the genesis of hydrocephalus, and 11 patients were previously reported with hydrocephalus and the syndrome of primary ciliary dyskinesia. primary ciliary dyskinesia–associated aqueductal stenosis should be considered as a possible cause for fetal or neonatal hydrocephalus if heterotaxy, heart malformations, and/or a probable genetic etiology are present.por
dc.identifier.citationJ Child Neurol. 2011 Oct 19por
dc.identifier.urihttp://hdl.handle.net/10400.17/1749
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherSAGE Publicationspor
dc.subjectTranstornos da Motilidade Ciliarpor
dc.subjectHidrocefaliapor
dc.subjectHDE NEU PEDpor
dc.titlePrimary Ciliary Dyskinesia and Hydrocephalus With Aqueductal Stenosispor
dc.typeconference object
dspace.entity.typePublication
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor

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