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Glucose-6-phosphate dehydrongenase deficiency is not a disease, it is an inherited disorder. It is a deficiency of the G6PD enzyme due to a error in your gene code you got from your parents. You can only lesson the severity of the symptoms and possible complications by educating yourself and others in order to help those you know that do have it. There are over 400 variants, some with obvious symptoms, some without. For the most up to date website go to: g5pddeficiency.org. Recent research shows the statistically, a lot more people are born with this deficiency than originally thought, many don't even know they, or a family member, has it until tragedy hits. Anyone can join (it's 100% free!). You will have access to the huge data base of contraindicated foods and substances. You can search the forum posts by subject, or post any question to the forum, and they will be answered by doctors and others that have done their homework, and really know their stuff!

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Why does g6pd deficiency prevent malaria?

G6PD or galactosemia.The baby is not able to metabolized galactose in the body causing mental retardation.Soy milk is recommended for this babies.


How many people died from G6PD?

G6PD deficiency is a genetic condition that can lead to severe complications such as hemolytic anemia. While this condition can be life-threatening, there isn't a specific number of deaths attributed solely to G6PD deficiency as it usually depends on other factors and individual health circumstances. Treatment and management can help prevent serious outcomes.


What Blood deficiency causes reactions to pain killers?

G6PD deficiency can cause reactions to painkillers.


What food are some people with G6PD deficiency allergic to?

Fava Beans


What are the symptoms of G6PD?

The most significant consequence of this disorder is hemolytic anemia, which is usually episodic, but the vast majority of people with G6PD deficiency have no symptoms.


Can g6pd deficiency occur in females?

Yes it can. Refer to g6pddeficiency.org for more information


Can women get G6PD deficiency?

G6pd Defiecienct is inherited from one or both of your parents. It cannot be passed from one person to another in any other way. Females can be carriers, G6pd deficient or unaffected. If both the mother and father are G6pd deficient then all their children will be g6pd deficient.


Is g6pd a disability?

G6PD deficiency is not considered a disability. It is a genetic condition that affects the enzyme responsible for protecting red blood cells from certain chemicals and stressors, leading to hemolytic anemia in some cases. With appropriate management and avoiding triggers, individuals with G6PD deficiency can lead healthy lives.


Can you use betadine if you have g6pd deficiency?

Yes, Betadine (povidone-iodine) can generally be used by individuals with G6PD deficiency, as it is not known to cause hemolytic reactions associated with this condition. However, it's essential to avoid excessive or prolonged use, as some individuals may have sensitivities. Always consult with a healthcare professional before using any antiseptic if you have G6PD deficiency or any other medical condition.


Can you take Mucinex if you have the G6pd deficiency?

Hello, This would be a good link for you to have...It has a list of what we can and can't take, eat or inhale with A Glucose 6 Phosphate Enzyme Deficiency. http://www.g6pd.org/favism/english/index.mvc?pgid=avoid


If you have G6PD deficiency fava beans will mess up your blood cells but it does make it less likely you'll get what disease?

Having G6PD deficiency increases the risk of hemolysis (destruction of red blood cells) when consuming fava beans. However, individuals with this deficiency are less likely to develop severe malaria because the parasite is less able to survive in red blood cells with reduced G6PD activity.


Is there a genetic test for deficiency of G6PD?

Yes. Direct DNA testing and sequencing of the G6PD gene are possible, and there is also a fast an inexpensive test called the "Beutler flourescent spot test" that can be performed on the blood of a patient suspected of having G6PD.