|
|
General
|
| |
Clinical Use:
|
G6PD deficiency is an inherited condition in which the body doesn't have enough G6PD, which helps red blood cells function normally. This deficiency can cause haemolytic anaemia, usually after exposure to certain medications, foods or even infections, and can cause prolonged neonatal jaundice. Most people with G6PD deficiency don't have any symptoms, while others develop symptoms of anaemia only after red blood cells have been destroyed. G6PD is one of many enzymes that help the body process carbohydrates and turn them into energy. G6PD also protects red blood cells from potentially harmful by-products that can accumulate when a person takes certain medications or when the body is fighting an infection. |
| |
Availability:
|
Samples are batched and tested twice a week.
Urgent and after hours testing is available with Duty Biochemist approval. |
| |
Aliases/Synonyms:
| G6P, |
| |
Code:
|
G6P |
| |
Handling Instructions (to laboratory):
|
Send sample chilled. |
| |
Hyperlink:
|
|
| |
Reference Interval:
|
0d to <3m: 12.5-35.0
3m to <120y: 8.2-25.0
|
Collection Requirements
|
| |
Container:
|
EDTA (LAVENDER), |
| |
Sample Type:
|
See container |
| |
Minimum Collection Volume:
|
20uL |
| |
Collection Instructions:
|
|
Processing Requirements
|
| |
Alternate Containers:
|
|
| |
Processing Instructions:
|
|
| |
Minimum Assay Volume:
|
|
| |
Stability:
|
7 days chilled |
| |
Transport Instructions (to testing laboratory):
|
Send sample chilled. |
Testing Locations
|
| |
Performed at:
|
|
Section
|
Department
|
Site
|
Contact Phone
|
| Special Chemistry |
Biochemistry |
QEII Medical Centre |
6383 4114 |
|
Last Updated : 16-09-2024 07:59 |