Treatment of pediatric burn patient having glucose-6-phosphate dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common red cell enzymopathy found in humans. It clearly has an X-linked recessive inheritance with its prevalence varying from 0% to 27% in a different caste, ethnic, and linguistic groups. This deficiency may result in hemolytic anemia...
Saved in:
Main Authors: | Vijay Y Bhatia (Author), Sankit D Shah (Author), Harshil Y Ravalji (Author), Deepa Banker (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2016-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Propofol infusion in an infant with glucose-6-phosphate dehydrogenase deficiency
by: Vandana Sharma, et al.
Published: (2018) -
Glucose-6-phosphate Dehydrogenase Deficiency: A Review
by: Nidhruv Ravikumar, et al.
Published: (2020) -
INCIDENCE OF ERYTHROCYTE GLUCOSE-6-PHOSPHATE- DEHYDROGENASE DEFICIENCY
by: Sh. Rahbar, et al.
Published: (1974) -
Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia
by: Ezzat Khodashenas, et al.
Published: (2015) -
Glucose-6-phosphate dehydrogenase (G6PD) Deficiency
by: DD Farhud, et al.
Published: (2008)