rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
5
|
pubmed:dateCreated |
1989-1-12
|
pubmed:abstractText |
The investigation and follow-up of three cases of EPP led us to reevaluate the signs and symptoms of the disease, the usefulness of early skin biopsies and protoporphyrin and ferrochelatase determinations. A review of the literature brought forth the salient features of this inborn error of porphyrin metabolism and stressed the value of treatment with beta-carotene and canthaxantine but also the risk of the so-called "gold dust" retinopathy.
|
pubmed:language |
fre
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0151-9638
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
115
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
555-60
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:3143300-Adult,
pubmed-meshheading:3143300-Canthaxanthin,
pubmed-meshheading:3143300-Carotenoids,
pubmed-meshheading:3143300-Child,
pubmed-meshheading:3143300-Erythrocytes,
pubmed-meshheading:3143300-Female,
pubmed-meshheading:3143300-Humans,
pubmed-meshheading:3143300-Male,
pubmed-meshheading:3143300-Porphyrias,
pubmed-meshheading:3143300-Porphyrins,
pubmed-meshheading:3143300-Protoporphyrins,
pubmed-meshheading:3143300-Skin,
pubmed-meshheading:3143300-Skin Diseases
|
pubmed:year |
1988
|
pubmed:articleTitle |
[Erythropoietic protoporphyria].
|
pubmed:affiliation |
Service de Dermatologie, Faculté de Médecine, Cliniques universitaires Saint-Luc, Bruxelles.
|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|