Document Detail


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

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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