| Autor: |
Kaplan M; Department of Neonatology, Shaare Zedek Medical Center, and the Faculty of Medicine of the Hebrew University, Jerusalem, Israel., Hammerman C, Vreman HJ, Stevenson DK, Beutler E |
| Jazyk: |
angličtina |
| Zdroj: |
The Journal of pediatrics [J Pediatr] 2001 Jul; Vol. 139 (1), pp. 137-40. |
| DOI: |
10.1067/mpd.2001.115312 |
| Abstrakt: |
Two premature female infants had severe hyperbilirubinemia caused by hemolysis. Both neonates were heterozygotes for the glucose-6-phosphate dehydrogenase Mediterranean mutation as determined by DNA analysis. Glucose-6-phosphate dehydrogenase-deficient heterozygotes may be susceptible to the complications of this enzyme deficiency. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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