Document Detail


A case of early myoclonic encephalopathy with the congenital nephrotic syndrome.
MedLine Citation:
PMID:  9105663     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We describe a male infant with early myoclonic encephalopathy (EME) associated with the congenital nephrotic syndrome, microcephaly, multiple minor anomalies, and cerebellar hypoplasia. He had erratic and massive myoclonus, and partial seizures from the neonatal period. Electroencephalography showed the so-called suppression-burst pattern. He died of disseminated intravascular coagulation caused by the congenital nephrotic syndrome at the age of two months. Our patients is the first reported case with EME associated with the congenital nephrotic syndrome.
Authors:
M Nishikawa; T Ichiyama; T Hayashi; S Furukawa
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Brain & development     Volume:  19     ISSN:  0387-7604     ISO Abbreviation:  Brain Dev.     Publication Date:  1997 Mar 
Date Detail:
Created Date:  1997-06-26     Completed Date:  1997-06-26     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7909235     Medline TA:  Brain Dev     Country:  NETHERLANDS    
Other Details:
Languages:  eng     Pagination:  144-7     Citation Subset:  IM    
Affiliation:
Department of Pediatrics, Yamaguchi University School of Medicine, Japan.
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple / radiography
Brain / radiography
Electroencephalography
Epilepsies, Myoclonic / complications*,  radiography
Fatal Outcome
Humans
Infant, Newborn
Male
Microcephaly / complications,  radiography
Nephrotic Syndrome / complications*,  congenital,  radiography
Tomography, X-Ray Computed

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


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