ملخص
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder characterized by low levels of the G6PD enzyme. It is present worldwide but with more prevalence in the Middle East and the Mediterranean areas. We report a case of severe hemolysis due to G6PD deficiency manifesting as methemoglobinemia in a 70 year old Omani male never known to have any previous hemolytic episodes or previously diagnosed of G6PD deficiency.
اللغة الأصلية | English |
---|---|
الصفحات (من إلى) | 135-137 |
عدد الصفحات | 3 |
دورية | Oman Medical Journal |
مستوى الصوت | 29 |
رقم الإصدار | 2 |
المعرِّفات الرقمية للأشياء | |
حالة النشر | Published - 2014 |
ASJC Scopus subject areas
- ???subjectarea.asjc.2700???