| Genetic basis of congenital nephrotic syndrome. | |
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MedLine Citation:
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PMID: 15018462 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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A young girl presented at 1 month of age with nephrotic syndrome. By incorporating clinical and pathologic data, the diagnosis of congenital nephrotic syndrome, Finnish type, was made. The differential diagnosis of early onset nephrotic syndrome, as it pertains to this patient is discussed. This article highlights recently discovered glomerular filtration proteins and their relationship to the pathophysiology of inherited kidney disease. |
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Authors:
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Laura S Finn |
Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society Volume: 6 ISSN: 1093-5266 ISO Abbreviation: Pediatr. Dev. Pathol. Publication Date: 2003 Nov-Dec |
Date Detail:
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Created Date: 2004-03-15 Completed Date: 2004-08-03 Revised Date: 2006-05-08 |
Medline Journal Info:
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Nlm Unique ID: 9809673 Medline TA: Pediatr Dev Pathol Country: United States |
Other Details:
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Languages: eng Pagination: 585-91 Citation Subset: IM |
Affiliation:
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Department of Laboratories, 6P-1, Children's Hospital and Regional Medical Center, 4800 Sand Point Way NE, Seattle, WA 98105, USA. lfinn@chmc.org |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Diagnosis, Differential Female Humans Infant, Newborn Kidney / pathology*, ultrastructure Microscopy, Electron Nephrotic Syndrome / congenital*, genetics*, physiopathology Proteinuria / etiology |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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