Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases.

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第一作者： Manu,Jamwal

第一单位： Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh 160012, India. Electronic address: manujamwal25@gmail.com.

作者： Manu,Jamwal ^[1] ; Anu,Aggarwal ^[2] ; Verinder,Kumar ^[3] ; Prashant,Sharma ^[4] ; Man Updesh Singh,Sachdeva ^[5] ; Deepak,Bansal ^[6] ; Pankaj,Malhotra ^[7] ; Reena,Das ^[8]

作者单位： Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh 160012, India. Electronic address: manujamwal25@gmail.com. ^[1] Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh 160012, India. Electronic address: aggarwalanu2011@gmail.com. ^[2] Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh 160012, India. Electronic address: verinderkumar@gmail.com. ^[3] Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh 160012, India. Electronic address: prashant.sh@gmail.com. ^[4] Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh 160012, India. Electronic address: drmanupdeshpgi@yahoo.co.in. ^[5] Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh 160012, India. Electronic address: deepakbansaldr@gmail.com. ^[6] Department of Internal Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh 160012, India. Electronic address: malhotrapankaj@hotmail.com. ^[7] Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh 160012, India. Electronic address: das.reena@pgimer.edu.in. ^[8]

关键词 Alpha gene deletion Gilbert syndrome Glucose-6-phosphate dehydrogenase deficiency Hereditary spherocytosis