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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1981-2-19
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pubmed:abstractText |
Hb A2 was determined in 50 subjects with erythrocyte G-6-PD deficiency who presented with hyperbilirubinemia in the neonatal period and in 100 non-hyperbilirubinemic G-6-PD deficient newborn infants, at the age of 12 months or more. Six subjects in the first group and 13 in the second were found to be carriers of the beta-thalassemia trait. Statistical analysis of the data did not show any significant difference between the two groups. It seems that the beta-thalassemia trait does not provide any protection against neonatal hyperbilirubinemia associated with G-6-PD deficiency.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0340-6199
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
134
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
119-20
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7439196-Glucosephosphate Dehydrogenase Deficiency,
pubmed-meshheading:7439196-Hemoglobin A2,
pubmed-meshheading:7439196-Heterozygote,
pubmed-meshheading:7439196-Humans,
pubmed-meshheading:7439196-Infant,
pubmed-meshheading:7439196-Infant, Newborn,
pubmed-meshheading:7439196-Jaundice, Neonatal,
pubmed-meshheading:7439196-Male,
pubmed-meshheading:7439196-Thalassemia
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pubmed:year |
1980
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pubmed:articleTitle |
beta-Thalassemia trait and hyperbilirubinemia in G-6-PD deficient newborn infants.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|