Human Factors Engineering Mutation and Hepcidin in Beta-Thalasseima - Saad El-dien, Sara Rabea Ibrahim;Badr, Eman Abd El-Fattah;El Sayed, Ibrahim El Tantawy
44,99 €
inkl. MwSt.
Versandkostenfrei*
Versandfertig in 6-10 Tagen
payback
22 °P sammeln
  • Broschiertes Buch

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 (Alzheimer's,Parkinson's, Huntington's), and premature death.

Andere Kunden interessierten sich auch für
Produktbeschreibung
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 (Alzheimer's,Parkinson's, Huntington's), 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