| Galloway-Mowat syndrome. | |
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MedLine Citation:
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PMID: 18798594 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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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. |
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Authors:
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Naureen Akhtar; Sadia Kiran; Farkhanda Hafeez |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Journal of the College of Physicians and Surgeons--Pakistan : JCPSP Volume: 18 ISSN: 1022-386X ISO Abbreviation: J Coll Physicians Surg Pak Publication Date: 2008 Aug |
Date Detail:
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Created Date: 2008-09-18 Completed Date: 2008-11-18 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9606447 Medline TA: J Coll Physicians Surg Pak Country: Pakistan |
Other Details:
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Languages: eng Pagination: 520-1 Citation Subset: IM |
Affiliation:
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Department of Paediatric Nephrology, The Children's Hospital and Institute of Child Health, Lahore, Pakistan. naureenakhtar@hotmail.com |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple
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genetics*,
pathology Child, Preschool Fetal Growth Retardation / genetics*, pathology Humans Male Microcephaly / genetics*, pathology Nephrotic Syndrome / genetics, pathology |
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