g6pd缺乏症简介（G6PD deficiency profile）.docVIP

g6pd缺乏症简介（G6PD deficiency profile） G6PD deficiency profile First, what is G6PD deficiency? G6PD deficiency is the abbreviation of glucose 6 phosphate deaminase deficiency. It is a hereditary hemolytic disease. There are two types of G6PD deficiency patients. One is G6PD who lacks hemolytic disease. Another is that G6PD lacks carriers of disease causing genes (which are inherited only to offspring and rarely attack themselves). Two, G6PD deficiency, what harm? G6PD deficiency patients from the number of men, only a few patients are female, about 400 million of the worlds population, national estimates of nearly one hundred million people is the lack of G6PD, so that you will understand it is a genetic disease how common, mild G6PD deficiency does not pay attention, because they can be completely as normal person. (but they can put the pathogenic genes to future generations), only special blood tests can be found, if you are lack of G6PD adults, you may take some drugs, or eat beans after symptoms appear, but G6PD deficiency babies are born in the first day of hemolytic jaundice, severe will the development of neonatal nuclear jaundice resulting in death or lifelong mental retardation. Three, G6PD lack of disease genes are transmitted to future generations? The G6PD gene is inherited X-linked manner. That is, if the father has this disease gene, and the mother is normal. All their daughters will inherit the gene, but the daughter is only the carrier of the gene. In general they do not get sick, but their children have the opportunity to get this half of the genetic gene, the couples son is completely normal; if the mother is positive, the pathogenic gene of father is normal, their children each have half a chance to get the gene, the genes son the incidence, the daughter of genes to future generations. Parents inherited disease causing genes from generation to generation. This is natural, life can change, this is genetic. Four, G6PD deficiency, why hemolysis occurs? T