Minucci Angelo, Concolino Paola, Antenucci Mirca, Santonocito Concetta, Ameglio Franco, Zuppi Cecilia, Giardina Bruno, Capoluongo Ettore
Laboratory of Clinical Molecular Biology, Department of Biochemistry and Clinical Biochemistry, Catholic University, Largo F Vito 1, 00168, Rome, Italy.
Clin Biochem. 2007 Aug;40(12):856-8. doi: 10.1016/j.clinbiochem.2007.03.025. Epub 2007 Apr 20.
We report a case of an asymptomatic young subject affected by severe deficiency of Glucose 6-phosphate dehydrogenase (G6PD) activity. A novel genetic mutation (G130A) in the third exon was found. We named this novel mutation the "G6PD RIGNANO variant". These findings may contribute to a better knowledge of molecular epidemiology of the G6PD mutation and may represent an additional variant to be studied for a deep comprehension of in vivo compensation mechanisms of G6PD deficiency.
我们报告了一例葡萄糖-6-磷酸脱氢酶(G6PD)活性严重缺乏的无症状年轻患者。在第三个外显子中发现了一种新的基因突变(G130A)。我们将这种新突变命名为“G6PD里尼亚诺变体”。这些发现可能有助于更好地了解G6PD突变的分子流行病学,并且可能代表一种有待研究的额外变体,以深入理解G6PD缺乏的体内补偿机制。