Screening for G6PD Deficiency in Neonates
Engy Adel Mohammed Abd El-Moneim;
Abstract
Introduction: G6PD deficiency is the most common enzyme
deficiency worldwide. It is an X-linked recessive disease,
affecting more than 400 million people worldwide. It causes a spectrum of diseases including neonatal hyperbilirubinemia, acute and chroni
deficiency worldwide. It is an X-linked recessive disease,
affecting more than 400 million people worldwide. It causes a spectrum of diseases including neonatal hyperbilirubinemia, acute and chroni
Other data
| Title | Screening for G6PD Deficiency in Neonates | Authors | Engy Adel Mohammed Abd El-Moneim | Keywords | Screening for G6PD Deficiency in Neonates | Issue Date | 2008 | Description | Introduction: G6PD deficiency is the most common enzyme deficiency worldwide. It is an X-linked recessive disease, affecting more than 400 million people worldwide. It causes a spectrum of diseases including neonatal hyperbilirubinemia, acute and chroni |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 9112C1134.pdf | 222.33 kB | Adobe PDF | View/Open |
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