Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
5
|
| pubmed:dateCreated |
1989-12-28
|
| pubmed:abstractText |
During investigation of chronic cyanosis in a 25 year old male, after excluding pulmonary and cardiac causes, methemoglobinemia was suspected. Investigation of the activity of methemoglobin reductase clenched the diagnosis of homozygous cytochrome b5 reductase deficiency in a case of recessive congenital methemoglobin type I (absence of neurologic symptoms).
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:author | |
| pubmed:volume |
31
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
371-3
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:2587207-Adult,
pubmed-meshheading:2587207-Cyanosis,
pubmed-meshheading:2587207-Cytochrome Reductases,
pubmed-meshheading:2587207-Cytochrome-B(5) Reductase,
pubmed-meshheading:2587207-Homozygote,
pubmed-meshheading:2587207-Humans,
pubmed-meshheading:2587207-Male,
pubmed-meshheading:2587207-NADH, NADPH Oxidoreductases,
pubmed-meshheading:2587207-Tunisia
|
| pubmed:year |
1989
|
| pubmed:articleTitle |
Congenital cyanosis due to methemoglobin reductase deficiency: first reported Tunisian case.
|
| pubmed:affiliation |
Hôpital Aziza Othmana, Service d'Hématologie, Tunis, Tunisie.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|