Infant Boy with Microcephaly Gastroesophageal Refl ux and Nephrotic Syndrome (Galloway-Mowat Syndrome): A Case Report.
dc.contributor.author | Malaki, M | |
dc.contributor.author | Rafeey, M | |
dc.date.accessioned | 2018-08-26T06:12:39Z | |
dc.date.available | 2018-08-26T06:12:39Z | |
dc.date.issued | 2012 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/42824 | |
dc.description.abstract | In 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.iso | English | |
dc.relation.ispartof | Middle East journal of digestive diseases | |
dc.title | Infant Boy with Microcephaly Gastroesophageal Refl ux and Nephrotic Syndrome (Galloway-Mowat Syndrome): A Case Report. | |
dc.type | article | |
dc.citation.volume | 4 | |
dc.citation.issue | 1 | |
dc.citation.spage | 51 | |
dc.citation.epage | 4 | |
dc.citation.index | Pubmed |
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