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Int J Clin Exp Pathol 2017;10(6):6552-6559 www.ijcep.com /ISSN:1936-2625/IJCEP0052924 Original Article Hereditary spherocytosis combined with glucose-6-phosphate dehydrogenase

Glucose-6-Phosphate Dehydrogenase DeficiencyLucio Luzzatto, MD, FRCP, FRCPatha,b,*, Caterina Nannelli, MScc, Rosario Notaro, MDc KEYWORDS KEY POINTS Glucose-6-phosphate dehydrogenase

A case report of a 4-year-old child with glucose-6-phosphate dehydrogenase deficiency: An evidence based approach to nutritional management Alex Pinto1, Anita MacDonald2,

02 G6PDAddress for correspondence and reprint requests: Professor Ainoon Othman, Haematology Unit, Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia,

Review The Possible Role of The Glucose-6-Phosphate Dehydrogenase Enzyme Deficiency in The Polyneuropathies Duygu Aydemir1,2 , Nuriye Nuray Ulusu1,2 1Koc University, School

02 G6PDAddress for correspondence and reprint requests: Professor Ainoon Othman, Haematology Unit, Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia,

Glucose-6-phosphate dehydrogenase (G6PD) mutations in Thailand: G6PD Viangchan (871G>A) is the most common deficiency variant in the Thai population © 2002 WILEY-LISS,

Singapore Med J 2009; 50 (1) : 62O r i g i n a l A r t i c l e Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Jalan Yaccob Latif, Kuala Lumpur

In Liaoning Province in northeastern China, we found a G6PD-deficient patient at the age of