G6PD deficiency题目 1. Which of the followings is the inheritance pattern of glucose-6-phosphate dehydrogenase (G6PD) deficiency? A. Autosomal dominant B. Autosomal recessive C. X-linked recessive D. Mitochondrial inheritance ANS: C 2. Which of the following statements is not true? a. G6PD deficiency is the most common human enzyme defect, being present in more than 400 million people worldwide. b. The most frequent clinical manifestations of G6PD deficiency are neonatal jaundice, and acute hemolytic anemia, which is usually triggered by an exogenous agent. c. G6PD is an enzyme that catalyzes the first reaction in glycolysis pathway. d. Most G6PD deficient individuals are asymptomatic throughout their life, and does not seem to be affected in life expectancy and quality of life. ANS: C (应该是 pentose phosphate pathway) 大家考试加油!! --

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