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RISK OF SEVERE JAUNDICE IN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY OF THE NEWBORN

✍ Scribed by Doxiadis, S.A.; Karaklis, A.; Valaes, T.; Stavrakakis, D.

Book ID
123473704
Publisher
The Lancet
Year
1964
Tongue
English
Weight
514 KB
Volume
284
Category
Article
ISSN
0140-6736

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Molecular mutations of the giucose-Cphosphate dehydrogenase (G6PD) gene and clinical manifestations of neonatal jaundice in 112 male and 50 female Chinese neonates with G6PD deficiency were studied. In the 112 males, the nucleotide (nt) 1376 (G-T) mutation was the dominant type (50.0%), followed by