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dc.contributor.authorMalaki, M
dc.contributor.authorRafeey, M
dc.date.accessioned2018-08-26T06:12:39Z
dc.date.available2018-08-26T06:12:39Z
dc.date.issued2012
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/42824
dc.description.abstractIn this case report, we present the first diagnosed case of Galloway-Mowat syndrome in Iran. A 7 month old infant boy withmicrocephaly that had prominently stunted head growth afterbirth, gastroesophageal reflux, multiple craniofascial characters,hypothyroidism and nephrotic syndrome diagnosed at 5 monthsof age associated with rapid decline in renal function and heavyproteinuria in 2 months .
dc.language.isoEnglish
dc.relation.ispartofMiddle East journal of digestive diseases
dc.titleInfant Boy with Microcephaly Gastroesophageal Refl ux and Nephrotic Syndrome (Galloway-Mowat Syndrome): A Case Report.
dc.typearticle
dc.citation.volume4
dc.citation.issue1
dc.citation.spage51
dc.citation.epage4
dc.citation.indexPubmed


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