Home About us Current issue Back issues Submission Instructions Advertise Contact Login   

Search Article 
  
Advanced search 
 
Saudi Journal of Kidney Diseases and Transplantation
Users online: 1864 Home Bookmark this page Print this page Email this page Small font sizeDefault font size Increase font size 

CASE REPORT Table of Contents   
Year : 1999  |  Volume : 10  |  Issue : 2  |  Page : 171-174
Late-Onset Nephrotic Syndrome in Galloway-Mowat Syndrome: A Case Report


Department of Pediatrics, King Hussein Medical Center, Amman, Jordan

Correspondence Address:
Issa Hazza
Department of Pediatric, King Hussein Medical Center, P.O. Box 960955, Amman 11196
Jordan
Login to access the Email id


PMID: 18212429

Rights and Permissions

Galloway-Mowat Syndrome (GMS) has a wide variety of clinical manifestations and histologic findings. All reported cases had developed nephrotic syndrome in the first two years of life. We report a case of 12 years old boy with microcephaly, mental retardation, and typical dysmorphic features of GMS with a late onset of minimal change nephritic syndrome which first manifested at seven years of age.


[FULL TEXT] [PDF]*
Print this article  Email this article
    

  Similar in PUBMED
    Search Pubmed for
    Search in Google Scholar for
   Citation Manager
  Access Statistics
   Reader Comments
   Email Alert *
   Add to My List *
 * Requires registration (Free)
 

 Article Access Statistics
    Viewed4117    
    Printed116    
    Emailed0    
    PDF Downloaded554    
    Comments [Add]    

Recommend this journal