Human Factors Engineering Mutation and Hepcidin in Beta-Thalasseima

Lieferzeit: Lieferbar innerhalb 14 Tagen

67,90 

Thalassemia, Hfe gene, Hereditary hemochromatosis, iron metabolism, hepcidin

ISBN: 6202308931
ISBN 13: 9786202308939
Autor: Saad El-dien, Sara Rabea Ibrahim/Badr, Eman Abd El-Fattah/El Sayed, Ibrahim El Tantawy
Verlag: Scholars‘ Press
Umfang: 140 S.
Erscheinungsdatum: 15.04.2018
Auflage: 1/2018
Format: 0.9 x 22 x 15
Gewicht: 227 g
Produktform: Kartoniert
Einband: Kartoniert
Artikelnummer: 5026382 Kategorie:

Beschreibung

Thalassemia is an important hematological disorder. The possibility of iron overload development may be increase by Interaction between thalassemia and HFE gene mutations. This study aim to investigate the possible association between serum hepcidin level as indicator of iron concentration and the presence of HFE gene mutations. Excess iron overload increases the risk of liver cirrhosis,cancer,hypogonadism,arthritis, cardiac arrhythmia, heart failure, retinal degeneration, diabetes mellitus, neurodegenerative diseases (Alzheimers,Parkinsons, Huntingtons), and premature death.

Autorenporträt

Dr.Sara R.Saad El-dien,Medical Analysis Specialist,Master in Biochemistry and Diploma in Analytical BioChemistry:Faculty of science Minufiya University.Prof.Eman.A.Badr,professor of Medical Biochemistry:Faculty of Medicine-Minufiya University.Prof.Ibrahim.E.El Sayed,Professor of Organic and Medicinal Chemistry:Faculty of Science-Minufiya University

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