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 you be around fire works if you have g6pd
G6PD (glucose-6-phosphate dehydrogenase) deficiency is a genetic condition that can lead to hemolytic anemia, particularly when an individual is exposed to certain triggers such as infections, medications, or certain foods. The deficiency results from mutations in the G6PD gene, which is crucial for protecting red blood cells from oxidative damage. Hyperbilirubinemia, an excess of bilirubin in the blood, can occur as a consequence of increased red blood cell breakdown in G6PD deficiency, leading to jaundice and other related symptoms. This condition is particularly common in males of African, Mediterranean, and Asian descent.
Anyone (male or female) with G6PD was BORN with it!People that are G6PD deficient are so because of a mutated gene on the X chromosome. In some cases, the symptoms do not appear later on in life as red cell production decreases; however, the person is deficient from conception, as their body is unable to to make any, or enough, g6pd. To put it in laymen's terms, G6PD is involved in a cellular process that helps your red blood cell's ability to fight oxidative stress. Too much stress, they die, and so can your body. However, if all foods, meds and other contraindicated substances are avoided (just like Superman avoided Kryptonite), most people can do quite well and live symptom free!For the most up to date and accurate information on the web concerning G6PD go to: g6pddeficiency.org
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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.
Tramadol is not on the list of contraindicated drugs for those with G6PD. Remember to always tell your doctor and pharmacist that you are G6PD Deficient and have them verify that the medicine is allowable for your use. An answer of 'probably' isn't really acceptable from a doctor making $300 an hour ;)
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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.
Ano po bawal Na karne SA may g6pd
G6PD or galactosemia.The baby is not able to metabolized galactose in the body causing mental retardation.Soy milk is recommended for this babies.