G-6PD Screening in Neonatal Hyperbilirubinemia
Glucose-6-Phosphate Dehydrogenase deficiency (G6PDD), is one of the commonest X-linked inherited erythroenzymopathy affecting 10% of the world population with a frequency of 0-27% in India. Children with G6PDD can develop acute haemolytic crises precipitated by particular foods or drugs causing sign...
Saved in:
Main Authors: | Suvitha Thilakarajan (Author), S.R Niveditha (Author), Keshavamurthy (Author) |
---|---|
Format: | Book |
Published: |
JCDR Research and Publications Pvt. Ltd.,
2015-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Neonatal Hyperbilirubinemia in infants with <it>G6PD c.563C > T</it><it>Variant</it>
by: Moiz Bushra, et al.
Published: (2012) -
G6PD genetic variations in neonatal Hyperbilirubinemia in Indonesian Deutromalay population
by: Dewi A. Wisnumurti, et al.
Published: (2019) -
Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong
by: Jia-Xin Xu, et al.
Published: (2021) -
The Genetics of Glucose-6-Phosphate-Dehydrogenase (G6PD) and Uridine Diphosphate Glucuronosyl Transferase 1A1 (UGT1A1) Promoter Gene Polymorphism in Relation to Quantitative Biochemical G6PD Activity Measurement and Neonatal Hyperbilirubinemia
by: Arieh Riskin, et al.
Published: (2023) -
Secondary Reporting of G6PD Deficiency on Newborn Screening
by: Stephanie C. Hoang, et al.
Published: (2023)