|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
8-9
|
|
pubmed:dateCreated |
2004-10-26
|
|
pubmed:abstractText |
Leucinosis (maple syrup urine disease) is a metabolic disorder caused by an enzymatic deficiency involved in the degradative pathways of the three branched-chain amino acids. We report an observation of acrodermatitis enteropathica-like syndrome induced by essential amino acid deficiency in a child with leucinosis.
|
|
pubmed:language |
fre
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:issn |
0151-9638
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
131
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
801-4
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:15505548-Acrodermatitis,
pubmed-meshheading:15505548-Genital Diseases, Male,
pubmed-meshheading:15505548-Humans,
pubmed-meshheading:15505548-Iatrogenic Disease,
pubmed-meshheading:15505548-Infant, Newborn,
pubmed-meshheading:15505548-Isoleucine,
pubmed-meshheading:15505548-Male,
pubmed-meshheading:15505548-Maple Syrup Urine Disease,
pubmed-meshheading:15505548-Mouth,
pubmed-meshheading:15505548-Syndrome
|
|
pubmed:articleTitle |
[Iatrogenic acrodermatitis enteropathica-like syndrome in leucinosis].
|
|
pubmed:affiliation |
Service de Dermatologie, CHU de Besançon, 2 place Saint-Jacques, 25030 Besançon, France.
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|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|
