18798594

Source:http://linkedlifedata.com/resource/pubmed/id/18798594

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0795949
pubmed:issue	8
pubmed:dateCreated	2008-9-18
pubmed:abstractText	Galloway-Mowat syndrome is a rare multisystem genetic disorder with constellation of neurological, skeletal, growth, facial, gastrointestinal and renal abnormalities. This case report describes Galloway-Mowat syndrome in a young boy suffering from congenital microcephaly, developmental delay, seizures and various dysmorphic features in whom nephrotic syndrome became apparent at 5 years of age.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9606447
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	1022-386X
pubmed:author	pubmed-author:AkhtarNaureenN, pubmed-author:HafeezFarkhandaF, pubmed-author:KiranSadiaS
pubmed:issnType	Print
pubmed:volume	18
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	520-1
pubmed:meshHeading	pubmed-meshheading:18798594-Abnormalities, Multiple, pubmed-meshheading:18798594-Child, Preschool, pubmed-meshheading:18798594-Fetal Growth Retardation, pubmed-meshheading:18798594-Humans, pubmed-meshheading:18798594-Male, pubmed-meshheading:18798594-Microcephaly, pubmed-meshheading:18798594-Nephrotic Syndrome
pubmed:year	2008
pubmed:articleTitle	Galloway-Mowat syndrome.
pubmed:affiliation	Department of Paediatric Nephrology, The Children's Hospital and Institute of Child Health, Lahore, Pakistan. naureenakhtar@hotmail.com
pubmed:publicationType	Journal Article, Case Reports